Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
GeneOntologyMolecularFunction	platelet-derived growth factor binding	COL2A1 COL1A1 COL1A2	3.33e-07	12	24	3	GO:0048407
GeneOntologyMolecularFunction	extracellular matrix structural constituent conferring tensile strength	COL2A1 COL1A1 COL1A2	2.24e-05	46	24	3	GO:0030020
GeneOntologyMolecularFunction	growth factor binding	COL2A1 COL1A1 COL1A2	8.39e-04	156	24	3	GO:0019838
GeneOntologyMolecularFunction	protease binding	ADAMTSL4 COL1A1 COL1A2	1.29e-03	181	24	3	GO:0002020
GeneOntologyMolecularFunction	extracellular matrix structural constituent	COL2A1 COL1A1 COL1A2	1.44e-03	188	24	3	GO:0005201
GeneOntologyBiologicalProcess	sensory perception of sound	COL2A1 TRIOBP CHD7 RIPOR2 COL1A1	3.52e-06	198	25	5	GO:0007605
GeneOntologyBiologicalProcess	sensory perception of mechanical stimulus	COL2A1 TRIOBP CHD7 RIPOR2 COL1A1	8.63e-06	238	25	5	GO:0050954
GeneOntologyBiologicalProcess	inner ear morphogenesis	COL2A1 TRIOBP CHD7 RIPOR2	1.67e-05	129	25	4	GO:0042472
GeneOntologyBiologicalProcess	ear morphogenesis	COL2A1 TRIOBP CHD7 RIPOR2	3.35e-05	154	25	4	GO:0042471
GeneOntologyBiologicalProcess	extracellular matrix organization	COL2A1 ZNF469 ADAMTSL4 COL1A1 COL1A2	7.81e-05	377	25	5	GO:0030198
GeneOntologyBiologicalProcess	extracellular structure organization	COL2A1 ZNF469 ADAMTSL4 COL1A1 COL1A2	7.91e-05	378	25	5	GO:0043062
GeneOntologyBiologicalProcess	external encapsulating structure organization	COL2A1 ZNF469 ADAMTSL4 COL1A1 COL1A2	8.01e-05	379	25	5	GO:0045229
GeneOntologyBiologicalProcess	collagen fibril organization	COL2A1 COL1A1 COL1A2	1.04e-04	76	25	3	GO:0030199
GeneOntologyBiologicalProcess	skin morphogenesis	COL1A1 COL1A2	1.47e-04	15	25	2	GO:0043589
GeneOntologyBiologicalProcess	embryo development	COL2A1 TRIOBP RRP7A CHD7 RIPOR2 CR1 INVS COL1A1	2.01e-04	1437	25	8	GO:0009790
GeneOntologyBiologicalProcess	inner ear development	COL2A1 TRIOBP CHD7 RIPOR2	2.28e-04	253	25	4	GO:0048839
GeneOntologyBiologicalProcess	negative regulation of innate immune response	ZDHHC18 SAMHD1 CR1	3.46e-04	114	25	3	GO:0045824
GeneOntologyBiologicalProcess	ear development	COL2A1 TRIOBP CHD7 RIPOR2	3.59e-04	285	25	4	GO:0043583
GeneOntologyBiologicalProcess	auditory receptor cell stereocilium organization	TRIOBP RIPOR2	4.50e-04	26	25	2	GO:0060088
GeneOntologyBiologicalProcess	embryonic organ development	COL2A1 TRIOBP CHD7 RIPOR2 INVS	4.95e-04	561	25	5	GO:0048568
GeneOntologyBiologicalProcess	auditory receptor cell morphogenesis	TRIOBP RIPOR2	6.42e-04	31	25	2	GO:0002093
GeneOntologyBiologicalProcess	sensory organ morphogenesis	COL2A1 TRIOBP CHD7 RIPOR2	7.21e-04	343	25	4	GO:0090596
GeneOntologyBiologicalProcess	skeletal system development	COL2A1 CHD7 ANO6 COL1A1 COL1A2	7.51e-04	615	25	5	GO:0001501
GeneOntologyBiologicalProcess	embryonic organ morphogenesis	COL2A1 TRIOBP CHD7 RIPOR2	7.86e-04	351	25	4	GO:0048562
GeneOntologyBiologicalProcess	negative regulation of response to biotic stimulus	ZDHHC18 SAMHD1 CR1	7.86e-04	151	25	3	GO:0002832
GeneOntologyBiologicalProcess	negative regulation of cell adhesion	RIPOR2 CR1 RCC2 COL1A1	1.01e-03	375	25	4	GO:0007162
GeneOntologyBiologicalProcess	auditory receptor cell development	TRIOBP RIPOR2	1.07e-03	40	25	2	GO:0060117
GeneOntologyBiologicalProcess	replacement ossification	COL2A1 COL1A1	1.24e-03	43	25	2	GO:0036075
GeneOntologyBiologicalProcess	endochondral ossification	COL2A1 COL1A1	1.24e-03	43	25	2	GO:0001958
GeneOntologyBiologicalProcess	microtubule-based process	RIPOR2 TTLL3 KIF13A KIAA1614 NSUN7 INVS	1.37e-03	1058	25	6	GO:0007017
GeneOntologyBiologicalProcess	cartilage development involved in endochondral bone morphogenesis	COL2A1 COL1A1	1.47e-03	47	25	2	GO:0060351
GeneOntologyCellularComponent	fibrillar collagen trimer	COL2A1 COL1A1 COL1A2	3.30e-07	12	25	3	GO:0005583
GeneOntologyCellularComponent	banded collagen fibril	COL2A1 COL1A1 COL1A2	3.30e-07	12	25	3	GO:0098643
GeneOntologyCellularComponent	collagen type I trimer	COL1A1 COL1A2	1.37e-06	2	25	2	GO:0005584
GeneOntologyCellularComponent	complex of collagen trimers	COL2A1 COL1A1 COL1A2	1.98e-06	21	25	3	GO:0098644
GeneOntologyCellularComponent	supramolecular fiber	COL2A1 TTLL3 KIF13A RCC2 CEP170B INVS COL1A1 COL1A2	4.56e-05	1179	25	8	GO:0099512
GeneOntologyCellularComponent	supramolecular polymer	COL2A1 TTLL3 KIF13A RCC2 CEP170B INVS COL1A1 COL1A2	4.79e-05	1187	25	8	GO:0099081
GeneOntologyCellularComponent	collagen trimer	COL2A1 COL1A1 COL1A2	1.55e-04	88	25	3	GO:0005581
GeneOntologyCellularComponent	microtubule	TTLL3 KIF13A RCC2 CEP170B INVS	3.68e-04	533	25	5	GO:0005874
GeneOntologyCellularComponent	endoplasmic reticulum lumen	COL2A1 ADAMTSL4 COL1A1 COL1A2	6.07e-04	332	25	4	GO:0005788
GeneOntologyCellularComponent	midbody	TRIOBP KIF13A RCC2	2.29e-03	222	25	3	GO:0030496
GeneOntologyCellularComponent	stereocilium	TRIOBP RIPOR2	3.07e-03	69	25	2	GO:0032420
GeneOntologyCellularComponent	collagen-containing extracellular matrix	COL2A1 ADAMTSL4 COL1A1 COL1A2	3.38e-03	530	25	4	GO:0062023
GeneOntologyCellularComponent	polymeric cytoskeletal fiber	TTLL3 KIF13A RCC2 CEP170B INVS	3.77e-03	899	25	5	GO:0099513
GeneOntologyCellularComponent	stereocilium bundle	TRIOBP RIPOR2	4.00e-03	79	25	2	GO:0032421
GeneOntologyCellularComponent	extracellular matrix	COL2A1 ADAMTSL4 COL1A1 COL1A2	7.19e-03	656	25	4	GO:0031012
GeneOntologyCellularComponent	external encapsulating structure	COL2A1 ADAMTSL4 COL1A1 COL1A2	7.27e-03	658	25	4	GO:0030312
HumanPheno	Joint subluxation	COL2A1 CHD7 COL1A1 COL1A2	5.37e-07	31	12	4	HP:0032153
HumanPheno	Neonatal short-limb short stature	COL2A1 COL1A1 COL1A2	3.58e-06	14	12	3	HP:0008921
HumanPheno	Biconcave flattened vertebrae	COL1A1 COL1A2	5.09e-06	2	12	2	HP:0003321
HumanPheno	Absent ossification of calvaria	COL1A1 COL1A2	5.09e-06	2	12	2	HP:0005623
HumanPheno	Severe generalized osteoporosis	COL1A1 COL1A2	5.09e-06	2	12	2	HP:0005897
HumanPheno	Femoral bowing present at birth, straightening with time	COL1A1 COL1A2	5.09e-06	2	12	2	HP:0005005
HumanPheno	Short limb dwarfism	COL2A1 COL1A1 COL1A2	9.48e-06	19	12	3	HP:0003505
HumanPheno	Generalized osteoporosis	COL2A1 COL1A1 COL1A2	1.11e-05	20	12	3	HP:0040160
HumanPheno	Dwarfism	COL2A1 COL1A1 COL1A2	1.30e-05	21	12	3	HP:0001516
HumanPheno	Popcorn calcification	COL1A1 COL1A2	1.52e-05	3	12	2	HP:6000871
HumanPheno	Dentinogenesis imperfecta	ZNF469 COL1A1 COL1A2	1.72e-05	23	12	3	HP:0000703
HumanPheno	Abnormal pulmonary valve physiology	ZNF469 CHD7 INVS COL1A1 COL1A2	2.08e-05	163	12	5	HP:0031654
HumanPheno	Biconcave vertebral bodies	COL2A1 COL1A1 COL1A2	2.23e-05	25	12	3	HP:0004586
HumanPheno	Abnormal dentin morphology	ZNF469 COL1A1 COL1A2	2.52e-05	26	12	3	HP:0010299
HumanPheno	Pulmonic regurgitation	INVS COL1A1 COL1A2	2.83e-05	27	12	3	HP:0010444
HumanPheno	Bowing of limbs due to multiple fractures	COL1A1 COL1A2	3.04e-05	4	12	2	HP:0003023
HumanPheno	Abnormality of habitus	COL2A1 ZNF469 CHD7 COL1A2	3.54e-05	87	12	4	HP:0010718
HumanPheno	Gracile long bones	COL2A1 ZNF469 COL1A1 COL1A2	3.87e-05	89	12	4	HP:0003061
HumanPheno	Slender long bone	COL2A1 ZNF469 COL1A1 COL1A2	3.87e-05	89	12	4	HP:0003100
HumanPheno	Avascular necrosis of the capital femoral epiphysis	COL2A1 COL1A1 COL1A2	3.91e-05	30	12	3	HP:0005743
HumanPheno	Basilar impression	COL1A1 COL1A2	5.07e-05	5	12	2	HP:0005758
HumanPheno	Bell-shaped thorax	COL2A1 COL1A1 COL1A2	5.24e-05	33	12	3	HP:0001591
HumanPheno	Abnormal pulmonary valve morphology	ZNF469 CHD7 INVS COL1A1 COL1A2	5.35e-05	198	12	5	HP:0001641
HumanPheno	Crumpled long bones	COL1A1 COL1A2	7.59e-05	6	12	2	HP:0006367
HumanPheno	Abnormal tibia morphology	COL2A1 CHD7 COL1A1 COL1A2	8.00e-05	107	12	4	HP:0002992
HumanPheno	Decreased skull ossification	COL2A1 COL1A1 COL1A2	8.71e-05	39	12	3	HP:0004331
HumanPheno	Disproportionate tall stature	COL2A1 ZNF469 COL1A2	1.01e-04	41	12	3	HP:0001519
HumanPheno	Tibial bowing	COL2A1 COL1A1 COL1A2	1.01e-04	41	12	3	HP:0002982
HumanPheno	Otosclerosis	COL1A1 COL1A2	1.06e-04	7	12	2	HP:0000362
HumanPheno	Molluscoid pseudotumors	ZNF469 COL1A1	1.06e-04	7	12	2	HP:0000993
HumanPheno	Juvenile aseptic necrosis	COL2A1 COL1A1 COL1A2	1.17e-04	43	12	3	HP:0100323
HumanPheno	Increased susceptibility to fractures	COL2A1 ZNF469 CHD7 COL1A1 COL1A2	1.22e-04	235	12	5	HP:0002659
HumanPheno	Soft skin	ZNF469 COL1A1 COL1A2	1.25e-04	44	12	3	HP:0000977
HumanPheno	Mitral valve prolapse	COL2A1 ZNF469 COL1A1 COL1A2	1.38e-04	123	12	4	HP:0001634
HumanPheno	Arterial rupture	COL1A1 COL1A2	1.41e-04	8	12	2	HP:0025019
HumanPheno	Generalized joint hypermobility	COL2A1 CHD7 COL1A1	1.63e-04	48	12	3	HP:0002761
HumanPheno	Thin ribs	COL2A1 COL1A1 COL1A2	2.07e-04	52	12	3	HP:0000883
HumanPheno	Joint laxity	COL2A1 CHD7 COL1A1	2.45e-04	55	12	3	HP:0001388
HumanPheno	Abnormal mitral valve morphology	COL2A1 ZNF469 COL1A1 COL1A2	2.68e-04	146	12	4	HP:0031477
HumanPheno	Abnormal epiphysis morphology	COL2A1 ZNF469 INVS COL1A1 COL1A2	2.74e-04	279	12	5	HP:0005930
HumanPheno	Multiple rib fractures	COL1A1 COL1A2	2.77e-04	11	12	2	HP:0006640
HumanPheno	Protrusio acetabuli	COL1A1 COL1A2	3.91e-04	13	12	2	HP:0003179
HumanPheno	Slender build	COL2A1 ZNF469 COL1A2	4.20e-04	66	12	3	HP:0001533
HumanPheno	Recurrent joint dislocation	COL1A1 COL1A2	4.56e-04	14	12	2	HP:0031869
HumanPheno	Severe hearing impairment	TRIOBP COL1A2	4.56e-04	14	12	2	HP:0012714
HumanPheno	Soft, doughy skin	COL1A1 COL1A2	4.56e-04	14	12	2	HP:0001027
HumanPheno	Aortic dilatation	SAMHD1 CHD7 COL1A1 COL1A2	4.59e-04	168	12	4	HP:0001724
HumanPheno	Aortic aneurysm	SAMHD1 CHD7 COL1A1 COL1A2	4.59e-04	168	12	4	HP:0004942
HumanPheno	Coxa vara	COL2A1 COL1A1 COL1A2	4.59e-04	68	12	3	HP:0002812
HumanPheno	Muscle flaccidity	COL1A1 COL1A2	5.25e-04	15	12	2	HP:0010547
HumanPheno	Osteoporosis	COL2A1 ZNF469 CHD7 COL1A1 COL1A2	5.51e-04	324	12	5	HP:0000939
HumanPheno	Atypical scarring of skin	ZNF469 COL1A1 COL1A2	5.89e-04	74	12	3	HP:0000987
HumanPheno	Abnormal stapes morphology	COL1A1 COL1A2	6.78e-04	17	12	2	HP:0008628
HumanPheno	Platybasia	COL1A1 COL1A2	6.78e-04	17	12	2	HP:0002691
HumanPheno	Decreased calvarial ossification	COL1A1 COL1A2	6.78e-04	17	12	2	HP:0005474
HumanPheno	Hallux valgus	ZNF469 COL1A1 COL1A2	7.41e-04	80	12	3	HP:0001822
HumanPheno	Multiple prenatal fractures	COL1A1 COL1A2	7.62e-04	18	12	2	HP:0005855
HumanPheno	Abnormal atrioventricular valve morphology	COL2A1 ZNF469 CHD7 COL1A1 COL1A2	7.87e-04	350	12	5	HP:0006705
HumanPheno	Abnormality of the epiphysis of the femoral head	COL2A1 COL1A1 COL1A2	8.25e-04	83	12	3	HP:0010574
HumanPheno	Abnormal femoral epiphysis morphology	COL2A1 COL1A1 COL1A2	9.16e-04	86	12	3	HP:0006499
HumanPheno	Joint stiffness	COL2A1 ADAMTSL4 COL1A1 COL1A2	9.25e-04	202	12	4	HP:0001387
HumanPheno	Spondylolisthesis	COL2A1 ZNF469	9.44e-04	20	12	2	HP:0003302
HumanPheno	Femoral hernia	COL1A1 COL1A2	9.44e-04	20	12	2	HP:0100541
HumanPheno	Shoulder dislocation	COL1A1 COL1A2	9.44e-04	20	12	2	HP:0003834
HumanPheno	Abnormal knee physiology	COL2A1 COL1A1 COL1A2	9.47e-04	87	12	3	HP:0034670
HumanPheno	Pes planus	COL2A1 ZNF469 CHD7 COL1A1 COL1A2	9.55e-04	365	12	5	HP:0001763
HumanPheno	Deviation of the hallux	ZNF469 COL1A1 COL1A2	9.79e-04	88	12	3	HP:0010051
HumanPheno	Abnormal epiphyseal ossification	COL2A1 COL1A1 COL1A2	9.79e-04	88	12	3	HP:0010656
HumanPheno	Abnormal hallux morphology	COL2A1 ZNF469 COL1A1 COL1A2	1.11e-03	212	12	4	HP:0001844
HumanPheno	Abnormal femoral head morphology	COL2A1 COL1A1 COL1A2	1.11e-03	92	12	3	HP:0003368
HumanPheno	Avascular necrosis	COL2A1 COL1A1 COL1A2	1.11e-03	92	12	3	HP:0010885
HumanPheno	Abnormal acetabulum morphology	COL2A1 COL1A1 COL1A2	1.11e-03	92	12	3	HP:0003170
HumanPheno	Coxa valga	COL2A1 COL1A1 COL1A2	1.11e-03	92	12	3	HP:0002673
HumanPheno	Abnormal heart valve morphology	COL2A1 ZNF469 CHD7 INVS COL1A1 COL1A2	1.15e-03	588	12	6	HP:0001654
HumanPheno	Vascular dilatation	SAMHD1 CHD7 COL1A1 COL1A2	1.17e-03	215	12	4	HP:0002617
HumanPheno	Abnormal lower limb epiphysis morphology	COL2A1 COL1A1 COL1A2	1.19e-03	94	12	3	HP:0006500
HumanPheno	High myopia	COL2A1 ZNF469 ADAMTSL4	1.19e-03	94	12	3	HP:0011003
HumanPheno	Enlarged thorax	COL2A1 COL1A1 COL1A2	1.19e-03	94	12	3	HP:0100625
HumanPheno	Abnormality of skull ossification	COL2A1 COL1A1 COL1A2	1.19e-03	94	12	3	HP:0002703
HumanPheno	Convex nasal ridge	SAMHD1 COL1A1 COL1A2	1.22e-03	95	12	3	HP:0000444
HumanPheno	Enchondroma	COL2A1 SAMHD1	1.25e-03	23	12	2	HP:0030038
HumanPheno	Abnormal foramen magnum morphology	COL1A1 COL1A2	1.25e-03	23	12	2	HP:0002699
HumanPheno	Upper extremity joint dislocation	CHD7 COL1A1 COL1A2	1.26e-03	96	12	3	HP:0030310
HumanPheno	Joint dislocation	COL2A1 ZNF469 CHD7 COL1A1 COL1A2	1.29e-03	390	12	5	HP:0001373
HumanPheno	Abnormality of the middle ear ossicles	COL1A1 COL1A2	1.48e-03	25	12	2	HP:0004452
HumanPheno	Abnormal heart valve physiology	ZNF469 CHD7 INVS COL1A1 COL1A2	1.50e-03	403	12	5	HP:0031653
HumanPheno	Scarring	ZNF469 COL1A1 COL1A2	1.50e-03	102	12	3	HP:0100699
HumanPheno	Abnormal 3rd finger morphology	COL2A1 COL1A1	1.60e-03	26	12	2	HP:0004150
HumanPheno	Abnormal tricuspid valve morphology	CHD7 COL1A1 COL1A2	1.64e-03	105	12	3	HP:0031440
HumanPheno	Dermal translucency	COL1A1 COL1A2	1.73e-03	27	12	2	HP:0010648
HumanPheno	Malar flattening	COL2A1 CHD7 ADAMTSL4 COL1A1	1.76e-03	240	12	4	HP:0000272
HumanPheno	Blue sclerae	ZNF469 COL1A1 COL1A2	1.77e-03	108	12	3	HP:0000592
HumanPheno	Disproportionate short-limb short stature	COL2A1 COL1A1 COL1A2	1.82e-03	109	12	3	HP:0008873
HumanPheno	Severe short stature	COL2A1 COL1A1 COL1A2	1.92e-03	111	12	3	HP:0003510
HumanPheno	Hip dysplasia	COL2A1 ZNF469 COL1A1 COL1A2	1.96e-03	247	12	4	HP:0001385
HumanPheno	Abnormal malar bone morphology	COL2A1 CHD7 ADAMTSL4 COL1A1	2.02e-03	249	12	4	HP:0012369
HumanPheno	Abnormal zygomatic arch morphology	COL2A1 CHD7 ADAMTSL4 COL1A1	2.05e-03	250	12	4	HP:0005557
HumanPheno	Abnormal zygomatic bone morphology	COL2A1 CHD7 ADAMTSL4 COL1A1	2.05e-03	250	12	4	HP:0010668
HumanPheno	Abnormal tricuspid valve morphology	CHD7 COL1A1 COL1A2	2.13e-03	115	12	3	HP:0001702
HumanPheno	Abnormal mitral valve morphology	COL2A1 ZNF469 COL1A1 COL1A2	2.27e-03	257	12	4	HP:0001633
MousePheno	impaired hearing	COL2A1 TRIOBP CHD7 RIPOR2 COL1A1	9.57e-06	223	19	5	MP:0006325
MousePheno	abnormal olecranon morphology	ANO6 COL1A1	1.05e-05	4	19	2	MP:0030856
MousePheno	abnormal compact bone lamellar structure	COL1A1 COL1A2	1.75e-05	5	19	2	MP:0010970
MousePheno	decreased tendon stiffness	COL1A1 COL1A2	1.75e-05	5	19	2	MP:0003098
MousePheno	abnormal synovial joint morphology	COL2A1 CHD7 COL1A1 COL1A2	2.06e-05	124	19	4	MP:0030804
MousePheno	abnormal tendon physiology	COL1A1 COL1A2	2.62e-05	6	19	2	MP:0030802
MousePheno	abnormal tendon stiffness	COL1A1 COL1A2	2.62e-05	6	19	2	MP:0003097
MousePheno	abnormal forelimb morphology	COL2A1 ANO6 COL1A1 COL1A2	9.25e-05	182	19	4	MP:0000550
MousePheno	decreased bone trabecula number	COL2A1 COL1A1 COL1A2	1.10e-04	70	19	3	MP:0010869
MousePheno	abnormal hearing physiology	COL2A1 TRIOBP CHD7 RIPOR2 KIF13A COL1A1	1.50e-04	643	19	6	MP:0001963
MousePheno	abnormal joint morphology	COL2A1 CHD7 ANO6 COL1A1 COL1A2	1.51e-04	397	19	5	MP:0002932
MousePheno	abnormal osteocyte morphology	COL1A1 COL1A2	1.82e-04	15	19	2	MP:0008753
MousePheno	abnormal ulna morphology	COL2A1 ANO6 COL1A1	1.89e-04	84	19	3	MP:0005108
MousePheno	decreased percent body fat/body weight	COL2A1 CHD7 COL1A1	1.89e-04	84	19	3	MP:0005459
MousePheno	abnormal ear physiology	COL2A1 TRIOBP CHD7 RIPOR2 KIF13A COL1A1	2.11e-04	684	19	6	MP:0003878
MousePheno	abnormal joint mobility	COL2A1 COL1A1	2.35e-04	17	19	2	MP:0008069
MousePheno	abnormal somatic nervous system morphology	COL2A1 TRIOBP CHD7 RIPOR2 TTLL3 RCC2 COL1A2	2.57e-04	1025	19	7	MP:0002752
MousePheno	abnormal osteocyte lacunocanalicular system morphology	COL1A1 COL1A2	2.64e-04	18	19	2	MP:0030485
MousePheno	small vertebral body	COL2A1 COL1A1	2.95e-04	19	19	2	MP:0004670
MousePheno	decreased bone volume	COL2A1 COL1A1 COL1A2	3.17e-04	100	19	3	MP:0010876
MousePheno	decreased embryonic neuroepithelium thickness	CHD7 ELOA2	3.28e-04	20	19	2	MP:0012703
MousePheno	abnormal forelimb zeugopod morphology	COL2A1 ANO6 COL1A1	3.36e-04	102	19	3	MP:0003855
MousePheno	delayed fertility	CHD7 COL1A1	3.62e-04	21	19	2	MP:0002683
MousePheno	short limbs	COL2A1 ANO6 COL1A1	4.30e-04	111	19	3	MP:0000547
MousePheno	abnormal primary cilium morphology	CHD7 TTLL3 INVS	4.65e-04	114	19	3	MP:0013203
MousePheno	abnormal thoracic cage shape	ANO6 COL1A1	4.75e-04	24	19	2	MP:0010099
MousePheno	abnormal limb joint morphology	COL2A1 COL1A2	5.15e-04	25	19	2	MP:0030805
MousePheno	abnormal trabecular bone morphology	COL2A1 ANO6 COL1A1 COL1A2	5.43e-04	289	19	4	MP:0000130
MousePheno	fragile skeleton	COL1A1 COL1A2	5.58e-04	26	19	2	MP:0000061
MousePheno	decreased cochlear hair cell stereocilia number	TRIOBP RIPOR2	5.58e-04	26	19	2	MP:0004523
MousePheno	abnormal compact bone thickness	COL2A1 COL1A1 COL1A2	5.67e-04	122	19	3	MP:0000134
MousePheno	abnormal cochlear inner hair cell morphology	TRIOBP CHD7 RIPOR2	5.95e-04	124	19	3	MP:0004393
MousePheno	short ribs	COL2A1 ANO6	6.48e-04	28	19	2	MP:0004672
MousePheno	delayed vaginal opening	CHD7 COL1A1	6.48e-04	28	19	2	MP:0002636
MousePheno	abnormal bone trabecula morphology	COL2A1 COL1A1 COL1A2	7.46e-04	134	19	3	MP:0010867
MousePheno	abnormal timing of vaginal opening	CHD7 COL1A1	7.95e-04	31	19	2	MP:0020150
MousePheno	abnormal tendon morphology	COL1A1 COL1A2	7.95e-04	31	19	2	MP:0005503
MousePheno	abnormal ocular fundus morphology	COL2A1 CHD7 TTLL3 CR1 ADAMTSL4 RCC2 COL1A2	9.15e-04	1262	19	7	MP:0002864
MousePheno	abnormal percent body fat/body weight	COL2A1 CHD7 COL1A1	9.19e-04	144	19	3	MP:0005457
MousePheno	hearing/vestibular/ear phenotype	COL2A1 TRIOBP CHD7 RIPOR2 KIF13A COL1A1	9.46e-04	905	19	6	MP:0005377
MousePheno	abnormal stationary movement	COL2A1 CHD7 COL1A1	9.76e-04	147	19	3	MP:0001388
MousePheno	decreased bone ossification	ANO6 COL1A1	1.13e-03	37	19	2	MP:0020040
MousePheno	decreased bone strength	COL1A1 COL1A2	1.20e-03	38	19	2	MP:0004991
MousePheno	abnormal susceptibility to hearing loss	CHD7 COL1A1	1.20e-03	38	19	2	MP:0006334
MousePheno	abnormal cochlear outer hair cell morphology	TRIOBP CHD7 RIPOR2	1.22e-03	159	19	3	MP:0004399
MousePheno	abnormal chest morphology	COL2A1 COL1A1	1.26e-03	39	19	2	MP:0004134
MousePheno	abnormal cochlear hair cell physiology	TRIOBP CHD7	1.32e-03	40	19	2	MP:0004432
MousePheno	abnormal scapula morphology	COL2A1 CHD7	1.32e-03	40	19	2	MP:0000149
MousePheno	absent distortion product otoacoustic emissions	CHD7 RIPOR2	1.39e-03	41	19	2	MP:0004737
MousePheno	abnormal face size	COL2A1 COL1A1	1.46e-03	42	19	2	MP:0030063
MousePheno	abnormal compact bone morphology	COL2A1 COL1A1 COL1A2	1.53e-03	172	19	3	MP:0003797
MousePheno	abnormal bone volume	COL2A1 COL1A1 COL1A2	1.56e-03	173	19	3	MP:0010874
MousePheno	hemorrhage	COL2A1 CHD7 INVS COL1A1 COL1A2	1.59e-03	664	19	5	MP:0001914
MousePheno	abnormal blood urea nitrogen level	CHD7 CR1 INVS COL1A2	1.64e-03	389	19	4	MP:0005265
MousePheno	abnormal inner hair cell stereociliary bundle morphology	TRIOBP RIPOR2	1.67e-03	45	19	2	MP:0004532
MousePheno	abnormal bone ossification	COL2A1 ANO6 COL1A1 COL1A2	1.74e-03	395	19	4	MP:0008271
MousePheno	abnormal bone mineralization	ANO6 COL1A1 COL1A2	1.78e-03	181	19	3	MP:0002896
MousePheno	abnormal hair cell physiology	TRIOBP CHD7	1.98e-03	49	19	2	MP:0003879
MousePheno	delayed sexual maturation	CHD7 COL1A1	1.98e-03	49	19	2	MP:0001938
MousePheno	abnormal uterus morphology	CHD7 CR1 KIF13A COL1A1	2.08e-03	415	19	4	MP:0001120
MousePheno	head bobbing	COL2A1 CHD7	2.14e-03	51	19	2	MP:0001410
MousePheno	decreased bone mineralization	ANO6 COL1A1	2.14e-03	51	19	2	MP:0020137
MousePheno	abnormal fibula morphology	COL2A1 COL1A1	2.14e-03	51	19	2	MP:0002187
MousePheno	abnormal anterior uvea morphology	COL2A1 CHD7 ADAMTSL4	2.33e-03	199	19	3	MP:0005194
MousePheno	abnormal nose morphology	COL2A1 CHD7 COL1A1	2.39e-03	201	19	3	MP:0002233
MousePheno	decreased circulating potassium level	CHD7 TTLL3	2.40e-03	54	19	2	MP:0005628
MousePheno	abnormal cochlear hair cell morphology	TRIOBP CHD7 RIPOR2	2.43e-03	202	19	3	MP:0002622
MousePheno	abnormal cilium morphology	CHD7 TTLL3 NSUN7 INVS	2.43e-03	433	19	4	MP:0013202
MousePheno	abnormal cochlear sensory epithelium morphology	TRIOBP CHD7 RIPOR2	2.60e-03	207	19	3	MP:0003308
MousePheno	abnormal organ of Corti morphology	TRIOBP CHD7 RIPOR2	2.68e-03	209	19	3	MP:0000042
MousePheno	abnormal femur morphology	COL2A1 COL1A1 COL1A2	2.86e-03	214	19	3	MP:0000559
MousePheno	abnormal hair cell morphology	TRIOBP CHD7 RIPOR2	2.86e-03	214	19	3	MP:0000045
MousePheno	abnormal hindlimb stylopod morphology	COL2A1 COL1A1 COL1A2	2.90e-03	215	19	3	MP:0003856
MousePheno	decreased trabecular bone volume	COL2A1 COL1A1	2.96e-03	60	19	2	MP:0010879
MousePheno	abnormal gastrulation	COL2A1 CHD7 ELOA2 INVS	3.25e-03	469	19	4	MP:0001695
Domain	Fib_collagen_C	COL2A1 COL1A1 COL1A2	4.41e-07	11	27	3	IPR000885
Domain	NC1_FIB	COL2A1 COL1A1 COL1A2	4.41e-07	11	27	3	PS51461
Domain	Fib_collagen_C	COL2A1 COL1A1 COL1A2	4.41e-07	11	27	3	PD002078
Domain	COLFI	COL2A1 COL1A1 COL1A2	4.41e-07	11	27	3	SM00038
Domain	COLFI	COL2A1 COL1A1 COL1A2	4.41e-07	11	27	3	PF01410
Domain	Collagen	COL2A1 COL1A1 COL1A2	2.46e-04	85	27	3	PF01391
Domain	Collagen	COL2A1 COL1A1 COL1A2	2.46e-04	85	27	3	IPR008160
Domain	FHA	KIF13A CEP170B	7.43e-04	28	27	2	SM00240
Domain	VWC	COL2A1 COL1A1	7.43e-04	28	27	2	PF00093
Domain	FHA_DOMAIN	KIF13A CEP170B	9.12e-04	31	27	2	PS50006
Domain	FHA	KIF13A CEP170B	9.12e-04	31	27	2	PF00498
Domain	FHA_dom	KIF13A CEP170B	1.23e-03	36	27	2	IPR000253
Domain	-	KIF13A CEP170B	1.23e-03	36	27	2	2.60.200.20
Domain	VWFC_1	COL2A1 COL1A1	1.23e-03	36	27	2	PS01208
Domain	VWC	COL2A1 COL1A1	1.37e-03	38	27	2	SM00214
Domain	VWFC_2	COL2A1 COL1A1	1.37e-03	38	27	2	PS50184
Domain	VWF_dom	COL2A1 COL1A1	1.67e-03	42	27	2	IPR001007
Domain	SMAD_FHA_domain	KIF13A CEP170B	2.55e-03	52	27	2	IPR008984
Domain	Ank_2	ANKS3 PPP1R12C INVS	3.59e-03	215	27	3	PF12796
Domain	TSP_1	THSD7B ADAMTSL4	3.72e-03	63	27	2	PF00090
Domain	TSP1_rpt	THSD7B ADAMTSL4	3.96e-03	65	27	2	IPR000884
Domain	TSP1	THSD7B ADAMTSL4	3.96e-03	65	27	2	PS50092
Domain	TSP1	THSD7B ADAMTSL4	3.96e-03	65	27	2	SM00209
Domain	Ank	ANKS3 PPP1R12C INVS	4.23e-03	228	27	3	PF00023
Domain	-	ANKS3 PPP1R12C INVS	5.35e-03	248	27	3	1.25.40.20
Domain	ANK	ANKS3 PPP1R12C INVS	5.53e-03	251	27	3	SM00248
Domain	ANK_REPEAT	ANKS3 PPP1R12C INVS	5.65e-03	253	27	3	PS50088
Domain	Ankyrin_rpt-contain_dom	ANKS3 PPP1R12C INVS	5.71e-03	254	27	3	IPR020683
Domain	ANK_REP_REGION	ANKS3 PPP1R12C INVS	5.71e-03	254	27	3	PS50297
Domain	Ankyrin_rpt	ANKS3 PPP1R12C INVS	6.22e-03	262	27	3	IPR002110
Domain	SAM	SAMHD1 ANKS3	7.14e-03	88	27	2	SM00454
Domain	SAM_DOMAIN	SAMHD1 ANKS3	8.27e-03	95	27	2	PS50105
Domain	SAM	SAMHD1 ANKS3	8.61e-03	97	27	2	IPR001660
Domain	-	SAMHD1 ANKS3	1.02e-02	106	27	2	1.10.150.50
Domain	SAM/pointed	SAMHD1 ANKS3	1.23e-02	117	27	2	IPR013761
Pathway	REACTOME_MET_ACTIVATES_PTK2_SIGNALING	COL2A1 COL1A1 COL1A2	1.98e-06	19	19	3	MM15512
Pathway	REACTOME_MET_ACTIVATES_PTK2_SIGNALING	COL2A1 COL1A1 COL1A2	8.24e-06	30	19	3	M27772
Pathway	REACTOME_MET_PROMOTES_CELL_MOTILITY	COL2A1 COL1A1 COL1A2	8.24e-06	30	19	3	MM15517
Pathway	REACTOME_NON_INTEGRIN_MEMBRANE_ECM_INTERACTIONS	COL2A1 COL1A1 COL1A2	1.00e-05	32	19	3	MM14924
Pathway	REACTOME_COLLAGEN_CHAIN_TRIMERIZATION	COL2A1 COL1A1 COL1A2	2.14e-05	41	19	3	MM15538
Pathway	REACTOME_MET_PROMOTES_CELL_MOTILITY	COL2A1 COL1A1 COL1A2	2.14e-05	41	19	3	M27778
Pathway	REACTOME_COLLAGEN_CHAIN_TRIMERIZATION	COL2A1 COL1A1 COL1A2	2.65e-05	44	19	3	M27812
Pathway	PID_SYNDECAN_1_PATHWAY	COL2A1 COL1A1 COL1A2	3.04e-05	46	19	3	M198
Pathway	REACTOME_ECM_PROTEOGLYCANS	COL2A1 COL1A1 COL1A2	3.24e-05	47	19	3	MM14925
Pathway	REACTOME_ENHANCED_BINDING_OF_GP1BA_VARIANT_TO_VWF_MULTIMER_COLLAGEN	COL1A1 COL1A2	3.60e-05	7	19	2	M48265
Pathway	REACTOME_ASSEMBLY_OF_COLLAGEN_FIBRILS_AND_OTHER_MULTIMERIC_STRUCTURES	COL2A1 COL1A1 COL1A2	3.91e-05	50	19	3	MM14796
Pathway	REACTOME_COLLAGEN_DEGRADATION	COL2A1 COL1A1 COL1A2	4.66e-05	53	19	3	MM14566
Pathway	REACTOME_DEFECTS_OF_PLATELET_ADHESION_TO_EXPOSED_COLLAGEN	COL1A1 COL1A2	4.80e-05	8	19	2	M48236
Pathway	REACTOME_NON_INTEGRIN_MEMBRANE_ECM_INTERACTIONS	COL2A1 COL1A1 COL1A2	6.43e-05	59	19	3	M27218
Pathway	REACTOME_ASSEMBLY_OF_COLLAGEN_FIBRILS_AND_OTHER_MULTIMERIC_STRUCTURES	COL2A1 COL1A1 COL1A2	7.11e-05	61	19	3	M27103
Pathway	REACTOME_COLLAGEN_BIOSYNTHESIS_AND_MODIFYING_ENZYMES	COL2A1 COL1A1 COL1A2	7.11e-05	61	19	3	MM14637
Pathway	REACTOME_COLLAGEN_DEGRADATION	COL2A1 COL1A1 COL1A2	8.21e-05	64	19	3	M26953
Pathway	PID_INTEGRIN1_PATHWAY	COL2A1 COL1A1 COL1A2	9.00e-05	66	19	3	M18
Pathway	REACTOME_COLLAGEN_BIOSYNTHESIS_AND_MODIFYING_ENZYMES	COL2A1 COL1A1 COL1A2	9.42e-05	67	19	3	M26999
Pathway	REACTOME_SIGNALING_BY_MET	COL2A1 COL1A1 COL1A2	9.42e-05	67	19	3	MM15345
Pathway	REACTOME_GP1B_IX_V_ACTIVATION_SIGNALLING	COL1A1 COL1A2	1.13e-04	12	19	2	MM15093
Pathway	REACTOME_PLATELET_ADHESION_TO_EXPOSED_COLLAGEN	COL1A1 COL1A2	1.13e-04	12	19	2	MM15452
Pathway	REACTOME_GP1B_IX_V_ACTIVATION_SIGNALLING	COL1A1 COL1A2	1.13e-04	12	19	2	M27352
Pathway	WP_FOCAL_ADHESION	COL2A1 PPP1R12C COL1A1 COL1A2	1.26e-04	199	19	4	M39402
Pathway	PID_AVB3_INTEGRIN_PATHWAY	COL2A1 COL1A1 COL1A2	1.27e-04	74	19	3	M160
Pathway	REACTOME_COLLAGEN_FORMATION	COL2A1 COL1A1 COL1A2	1.37e-04	76	19	3	MM14573
Pathway	REACTOME_ECM_PROTEOGLYCANS	COL2A1 COL1A1 COL1A2	1.37e-04	76	19	3	M27219
Pathway	REACTOME_INTEGRIN_CELL_SURFACE_INTERACTIONS	COL2A1 COL1A1 COL1A2	1.37e-04	76	19	3	MM14867
Pathway	REACTOME_SIGNALING_BY_MET	COL2A1 COL1A1 COL1A2	1.54e-04	79	19	3	M27643
Pathway	REACTOME_ANCHORING_FIBRIL_FORMATION	COL1A1 COL1A2	1.79e-04	15	19	2	M27161
Pathway	KEGG_ECM_RECEPTOR_INTERACTION	COL2A1 COL1A1 COL1A2	1.85e-04	84	19	3	M7098
Pathway	REACTOME_INTEGRIN_CELL_SURFACE_INTERACTIONS	COL2A1 COL1A1 COL1A2	1.91e-04	85	19	3	M16441
Pathway	REACTOME_PLATELET_ADHESION_TO_EXPOSED_COLLAGEN	COL1A1 COL1A2	2.04e-04	16	19	2	M9450
Pathway	REACTOME_COLLAGEN_FORMATION	COL2A1 COL1A1 COL1A2	2.26e-04	90	19	3	M631
Pathway	REACTOME_CROSSLINKING_OF_COLLAGEN_FIBRILS	COL1A1 COL1A2	2.60e-04	18	19	2	M27164
Pathway	REACTOME_CROSSLINKING_OF_COLLAGEN_FIBRILS	COL1A1 COL1A2	2.60e-04	18	19	2	MM14882
Pathway	REACTOME_DISEASES_OF_HEMOSTASIS	COL1A1 COL1A2	2.90e-04	19	19	2	M48230
Pathway	REACTOME_SCAVENGING_BY_CLASS_A_RECEPTORS	COL1A1 COL1A2	2.90e-04	19	19	2	M27221
Pathway	REACTOME_DEGRADATION_OF_THE_EXTRACELLULAR_MATRIX	COL2A1 COL1A1 COL1A2	4.54e-04	114	19	3	MM14571
Pathway	PID_LYMPH_ANGIOGENESIS_PATHWAY	COL1A1 COL1A2	5.07e-04	25	19	2	M274
Pathway	REACTOME_SYNDECAN_INTERACTIONS	COL1A1 COL1A2	5.92e-04	27	19	2	M27217
Pathway	WP_DYSREGULATED_MIRNA_TARGETING_IN_INSULINPI3KAKT_SIGNALING	COL1A1 COL1A2	6.37e-04	28	19	2	MM15957
Pathway	WP_ANGIOTENSIN_II_RECEPTOR_TYPE_1_PATHWAY	COL1A1 COL1A2	6.37e-04	28	19	2	M42541
Pathway	WP_INFLAMMATORY_RESPONSE_PATHWAY	COL1A1 COL1A2	7.32e-04	30	19	2	MM15812
Pathway	WP_INFLAMMATORY_RESPONSE_PATHWAY	COL1A1 COL1A2	7.32e-04	30	19	2	M39641
Pathway	REACTOME_IMMUNOREGULATORY_INTERACTIONS_BETWEEN_A_LYMPHOID_AND_A_NON_LYMPHOID_CELL	COL2A1 COL1A1 COL1A2	7.44e-04	135	19	3	MM14781
Pathway	REACTOME_DEGRADATION_OF_THE_EXTRACELLULAR_MATRIX	COL2A1 COL1A1 COL1A2	8.27e-04	140	19	3	M587
Pathway	WP_TYPE_I_COLLAGEN_SYNTHESIS_IN_THE_CONTEXT_OF_OSTEOGENESIS_IMPERFECTA	COL1A1 COL1A2	8.86e-04	33	19	2	M39870
Pathway	REACTOME_GPVI_MEDIATED_ACTIVATION_CASCADE	COL1A1 COL1A2	9.97e-04	35	19	2	MM14512
Pathway	REACTOME_GPVI_MEDIATED_ACTIVATION_CASCADE	COL1A1 COL1A2	9.97e-04	35	19	2	M773
Pathway	REACTOME_PLATELET_AGGREGATION_PLUG_FORMATION	COL1A1 COL1A2	1.18e-03	38	19	2	MM15456
Pathway	REACTOME_PLATELET_AGGREGATION_PLUG_FORMATION	COL1A1 COL1A2	1.24e-03	39	19	2	M10735
Pathway	REACTOME_O_GLYCOSYLATION_OF_TSR_DOMAIN_CONTAINING_PROTEINS	THSD7B ADAMTSL4	1.24e-03	39	19	2	M27417
Pathway	REACTOME_O_GLYCOSYLATION_OF_TSR_DOMAIN_CONTAINING_PROTEINS	THSD7B ADAMTSL4	1.24e-03	39	19	2	MM15165
Pathway	PID_INTEGRIN3_PATHWAY	COL1A1 COL1A2	1.50e-03	43	19	2	M53
Pathway	WP_FOCAL_ADHESION	COL2A1 COL1A1 COL1A2	1.90e-03	187	19	3	MM15913
Pathway	REACTOME_IMMUNOREGULATORY_INTERACTIONS_BETWEEN_A_LYMPHOID_AND_A_NON_LYMPHOID_CELL	COL2A1 COL1A1 COL1A2	1.99e-03	190	19	3	M8240
Pathway	WP_OSTEOARTHRITIC_CHONDROCYTE_HYPERTROPHY	COL2A1 COL1A1	2.03e-03	50	19	2	M48087
Pathway	KEGG_FOCAL_ADHESION	COL2A1 COL1A1 COL1A2	2.27e-03	199	19	3	M7253
Pathway	WP_NRP1TRIGGERED_SIGNALING_IN_PANCREATIC_CANCER	COL1A1 COL1A2	2.36e-03	54	19	2	M42568
Pathway	REACTOME_SENSORY_PROCESSING_OF_SOUND_BY_OUTER_HAIR_CELLS_OF_THE_COCHLEA	TRIOBP RIPOR2	2.45e-03	55	19	2	M41823
Pathway	PID_IL4_2PATHWAY	COL1A1 COL1A2	3.30e-03	64	19	2	M28
Pathway	REACTOME_DISEASES_ASSOCIATED_WITH_O_GLYCOSYLATION_OF_PROTEINS	THSD7B ADAMTSL4	3.72e-03	68	19	2	M27303
Pathway	WP_UROTENSINIIMEDIATED_SIGNALING	COL2A1 COL1A1	3.83e-03	69	19	2	M48052
Pathway	REACTOME_EXTRACELLULAR_MATRIX_ORGANIZATION	COL2A1 COL1A1 COL1A2	4.73e-03	258	19	3	MM14572
Pathway	REACTOME_SENSORY_PROCESSING_OF_SOUND	TRIOBP RIPOR2	4.74e-03	77	19	2	M41822
Pathway	REACTOME_EXTRACELLULAR_MATRIX_ORGANIZATION	COL2A1 COL1A1 COL1A2	7.18e-03	300	19	3	M610
Pathway	WP_FOCAL_ADHESION_PI3KAKTMTORSIGNALING	COL2A1 COL1A1 COL1A2	7.31e-03	302	19	3	M39719
Pathway	REACTOME_BINDING_AND_UPTAKE_OF_LIGANDS_BY_SCAVENGER_RECEPTORS	COL1A1 COL1A2	7.57e-03	98	19	2	M27152
Pathway	WP_FOCAL_ADHESION_PI3KAKTMTOR_SIGNALING_PATHWAY	COL2A1 COL1A1 COL1A2	9.02e-03	326	19	3	MM15917
Pathway	REACTOME_O_LINKED_GLYCOSYLATION	THSD7B ADAMTSL4	9.30e-03	109	19	2	MM15164
Pathway	WP_COMPREHENSIVE_IL17A_SIGNALING	SAMHD1 COL1A1	9.46e-03	110	19	2	MM16642
Pathway	REACTOME_O_LINKED_GLYCOSYLATION	THSD7B ADAMTSL4	9.63e-03	111	19	2	M27416
Pathway	WP_BURN_WOUND_HEALING	COL1A1 COL1A2	9.96e-03	113	19	2	M42571
Pathway	WP_PI3KAKT_SIGNALING	COL2A1 COL1A1 COL1A2	1.00e-02	339	19	3	M39736
Pathway	REACTOME_DISEASES_OF_GLYCOSYLATION	THSD7B ADAMTSL4	1.56e-02	143	19	2	M27275
Pathway	REACTOME_SIGNALING_BY_RECEPTOR_TYROSINE_KINASES	COL2A1 COL1A1 COL1A2	1.76e-02	418	19	3	MM15587
Pubmed	Molecular response of human cervical and lumbar nucleus pulposus cells from degenerated discs following cytokine treatment.	COL2A1 COL1A1 COL1A2	4.17e-10	3	27	3	23546968
Pubmed	Mutations in collagen genes: causes of rare and some common diseases in humans.	COL2A1 COL1A1 COL1A2	4.17e-10	3	27	3	2010058
Pubmed	Upstream elements present in the 3'-untranslated region of collagen genes influence the processing efficiency of overlapping polyadenylation signals.	COL2A1 COL1A1 COL1A2	4.17e-10	3	27	3	12200454
Pubmed	Immunohistochemical characteristics of developing mandibular angle in fetal mice.	COL2A1 COL1A1 COL1A2	1.67e-09	4	27	3	16356873
Pubmed	Expression and localization of collagen-binding stress protein Hsp47 in mouse embryo development: comparison with types I and II collagen.	COL2A1 COL1A1 COL1A2	1.67e-09	4	27	3	9880238
Pubmed	Two novel sites of expression of NADPH cytochrome P450 reductase during murine embryogenesis: limb mesenchyme and developing olfactory neuroepithelia.	COL2A1 COL1A1 COL1A2	1.67e-09	4	27	3	10633870
Pubmed	Transcriptional link between blood and bone: the stem cell leukemia gene and its +19 stem cell enhancer are active in bone cells.	COL2A1 COL1A1 COL1A2	1.67e-09	4	27	3	16537906
Pubmed	Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels.	COL2A1 COL1A1 COL1A2	8.33e-09	6	27	3	9101290
Pubmed	Development and regeneration of the neonatal digit tip in mice.	COL2A1 COL1A1 COL1A2	8.33e-09	6	27	3	18234177
Pubmed	Regulation of chondrocyte differentiation by Cbfa1.	COL2A1 COL1A1 COL1A2	1.46e-08	7	27	3	10072783
Pubmed	Formation and maturation of the murine meniscus.	COL2A1 COL1A1 COL1A2	2.33e-08	8	27	3	27664939
Pubmed	Filamin B mutations cause chondrocyte defects in skeletal development.	COL2A1 COL1A1 COL1A2	2.33e-08	8	27	3	17510210
Pubmed	Type XIII collagen strongly affects bone formation in transgenic mice.	COL2A1 COL1A1 COL1A2	2.33e-08	8	27	3	16007336
Pubmed	Augmented Indian hedgehog signaling in cranial neural crest cells leads to craniofacial abnormalities and dysplastic temporomandibular joint in mice.	COL2A1 COL1A1 COL1A2	2.33e-08	8	27	3	26553654
Pubmed	Type I, II, III, IV, V, and VI collagens serve as extracellular ligands for the isoforms of platelet-derived growth factor (AA, BB, and AB).	COL2A1 COL1A1 COL1A2	3.49e-08	9	27	3	8900172
Pubmed	Neutral Sphingomyelinase 2 (SMPD3) Deficiency in Mice Causes Chondrodysplasia with Unimpaired Skeletal Mineralization.	COL2A1 COL1A1 COL1A2	3.49e-08	9	27	3	31199918
Pubmed	Development of heart valve leaflets and supporting apparatus in chicken and mouse embryos.	COL2A1 COL1A1 COL1A2	4.99e-08	10	27	3	15162503
Pubmed	Ucma is not necessary for normal development of the mouse skeleton.	COL2A1 COL1A1 COL1A2	4.99e-08	10	27	3	22155508
Pubmed	VEGF stimulates intramembranous bone formation during craniofacial skeletal development.	COL2A1 COL1A1 COL1A2	4.99e-08	10	27	3	26899202
Pubmed	Involvement of endogenous bone morphogenetic protein (BMP) 2 and BMP6 in bone formation.	COL2A1 COL1A1 COL1A2	4.99e-08	10	27	3	16109715
Pubmed	ER, Mitochondria, and ISR Regulation by mt-HSP70 and ATF5 upon Procollagen Misfolding in Osteoblasts.	COL2A1 COL1A1 COL1A2	6.86e-08	11	27	3	35988140
Pubmed	Hsp and chaperone distribution during endochondral bone development in mouse embryo.	COL2A1 COL1A1 COL1A2	6.86e-08	11	27	3	9880236
Pubmed	Replacing Shox2 with human SHOX leads to congenital disc degeneration of the temporomandibular joint in mice.	COL2A1 COL1A1 COL1A2	6.86e-08	11	27	3	24248941
Pubmed	Mouse fibroblast growth factor 9 N143T mutation leads to wide chondrogenic condensation of long bones.	COL2A1 COL1A1 COL1A2	9.14e-08	12	27	3	32002646
Pubmed	Overexpression of BMP3 in the developing skeleton alters endochondral bone formation resulting in spontaneous rib fractures.	COL2A1 COL1A1 COL1A2	1.19e-07	13	27	3	19653325
Pubmed	Ultrastructural cartilage abnormalities in MIA/CD-RAP-deficient mice.	COL2A1 COL1A1 COL1A2	1.19e-07	13	27	3	11839810
Pubmed	Arp2/3 inactivation causes intervertebral disc and cartilage degeneration with dysregulated TonEBP-mediated osmoadaptation.	COL2A1 COL1A1 COL1A2	1.19e-07	13	27	3	31961823
Pubmed	Craniofacial abnormality with skeletal dysplasia in mice lacking chondroitin sulfate N-acetylgalactosaminyltransferase-1.	COL2A1 COL1A1 COL1A2	1.51e-07	14	27	3	30459452
Pubmed	Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis.	COL2A1 COL1A1 COL1A2	1.51e-07	14	27	3	17194222
Pubmed	Collagen II is essential for the removal of the notochord and the formation of intervertebral discs.	COL2A1 COL1A1 COL1A2	1.89e-07	15	27	3	9832566
Pubmed	Extracellular Matrix Disorganization Caused by ADAMTS16 Deficiency Leads to Bicuspid Aortic Valve With Raphe Formation.	COL2A1 COL1A1 COL1A2	1.89e-07	15	27	3	38018454
Pubmed	Enhanced BMP signaling leads to enlarged nasal cartilage formation in mice.	COL2A1 COL1A1 COL1A2	2.32e-07	16	27	3	37640003
Pubmed	Synovial joint formation requires local Ext1 expression and heparan sulfate production in developing mouse embryo limbs and spine.	COL2A1 COL1A1 COL1A2	2.82e-07	17	27	3	21185280
Pubmed	SIK3 is essential for chondrocyte hypertrophy during skeletal development in mice.	COL2A1 COL1A1 COL1A2	2.82e-07	17	27	3	22318228
Pubmed	Loss of Foxc1 and Foxc2 function in chondroprogenitor cells disrupts endochondral ossification.	COL2A1 COL1A1 COL1A2	2.82e-07	17	27	3	34331943
Pubmed	Long bone development requires a threshold of Hox function.	COL2A1 COL1A1 COL1A2	2.82e-07	17	27	3	24930703
Pubmed	Wnt/beta-catenin signaling in mesenchymal progenitors controls osteoblast and chondrocyte differentiation during vertebrate skeletogenesis.	COL2A1 COL1A1 COL1A2	4.01e-07	19	27	3	15866164
Pubmed	Site-1 protease is essential for endochondral bone formation in mice.	COL2A1 COL1A1 COL1A2	4.01e-07	19	27	3	18025304
Pubmed	Indian hedgehog synchronizes skeletal angiogenesis and perichondrial maturation with cartilage development.	COL2A1 COL1A1 COL1A2	4.01e-07	19	27	3	15689378
Pubmed	The role of macrophages in the disappearance of Meckel's cartilage during mandibular development in mice.	COL2A1 COL1A1 COL1A2	4.71e-07	20	27	3	19853894
Pubmed	Site-1 protease regulates skeletal stem cell population and osteogenic differentiation in mice.	COL2A1 COL1A1 COL1A2	4.71e-07	20	27	3	29437042
Pubmed	Smad4 is required to induce digit ray primordia and to initiate the aggregation and differentiation of chondrogenic progenitors in mouse limb buds.	COL2A1 COL1A1 COL1A2	5.50e-07	21	27	3	23034633
Pubmed	Complete primary structure of rainbow trout type I collagen consisting of alpha1(I)alpha2(I)alpha3(I) heterotrimers.	COL1A1 COL1A2	5.80e-07	2	27	2	11358497
Pubmed	Regulation of type I collagen genes expression.	COL1A1 COL1A2	5.80e-07	2	27	2	11143996
Pubmed	No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women.	COL1A1 COL1A2	5.80e-07	2	27	2	21602843
Pubmed	Age-related trends and reference intervals of cross-linked C-telopeptide of type I collagen and procollagen type I N-propeptide from a reference population of Sri Lankan adult women.	COL1A1 COL1A2	5.80e-07	2	27	2	34727246
Pubmed	Proposed association between the COL1A1 and COL1A2 genes and otosclerosis is not supported by a case-control study in Spain.	COL1A1 COL1A2	5.80e-07	2	27	2	15211650
Pubmed	Identification of COL1A1 and COL1A2 as candidate prognostic factors in gastric cancer.	COL1A1 COL1A2	5.80e-07	2	27	2	27894325
Pubmed	COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus.	COL2A1 COL1A1	5.80e-07	2	27	2	19387081
Pubmed	Isolation and characterization of genomic clones corresponding to the human type II procollagen gene.	COL2A1 COL1A1	5.80e-07	2	27	2	6320112
Pubmed	[Expression and clinical significance of COL1A1 and COL1A2 genes in malignant pleural mesothelioma tissues].	COL1A1 COL1A2	5.80e-07	2	27	2	35915937
Pubmed	Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - genotype-phenotype correlations and effect of bisphosphonate treatment.	COL1A1 COL1A2	5.80e-07	2	27	2	26927310
Pubmed	Osteogenesis imperfecta: mosaicism and refinement of the genotype-phenotype map in OI type III. Mutations in brief no. 242. Online.	COL1A1 COL1A2	5.80e-07	2	27	2	10408781
Pubmed	Characterization of point mutations in the collagen COL1A1 and COL1A2 genes causing lethal perinatal osteogenesis imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	2777764
Pubmed	[Phenotype-genotype analysis and detection of gene variant in six families with osteogenesis imperfecta].	COL1A1 COL1A2	5.80e-07	2	27	2	32335875
Pubmed	Collagen gene polymorphisms influence fracture risk and bone mass acquisition during childhood and adolescent growth.	COL1A1 COL1A2	5.80e-07	2	27	2	20736093
Pubmed	[Analysis of COL1A1 and COL1A2 gene variants in two fetuses with osteogenesis imperfecta].	COL1A1 COL1A2	5.80e-07	2	27	2	37368383
Pubmed	Streptococcal protein FOG, a novel matrix adhesin interacting with collagen I in vivo.	COL1A1 COL1A2	5.80e-07	2	27	2	16278217
Pubmed	Osteogenesis imperfecta: comparison of molecular defects with bone histological changes.	COL1A1 COL1A2	5.80e-07	2	27	2	7520724
Pubmed	Mutation in the carboxy-terminal propeptide of the Pro alpha 1(I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): possible implications for protein folding.	COL1A1 COL1A2	5.80e-07	2	27	2	8723681
Pubmed	Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	36951356
Pubmed	Effects of GABA on the expression of type I collagen gene in normal human dermal fibroblasts.	COL1A1 COL1A2	5.80e-07	2	27	2	27691923
Pubmed	Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood.	COL1A1 COL1A2	5.80e-07	2	27	2	17211858
Pubmed	Identification of COL1A1/2 Mutations and Fusions With Noncoding RNA Genes in Bizarre Parosteal Osteochondromatous Proliferation (Nora Lesion).	COL1A1 COL1A2	5.80e-07	2	27	2	36853784
Pubmed	Serine for glycine substitutions in type I collagen in two cases of type IV osteogenesis imperfecta (OI). Additional evidence for a regional model of OI pathophysiology.	COL1A1 COL1A2	5.80e-07	2	27	2	8094076
Pubmed	Inter- and Intrafamilial Phenotypic Variability in Individuals with Collagen-Related Osteogenesis Imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	32166892
Pubmed	Isolation and characterization of the cyanogen bromide peptides from the alpha 1 and alpha 2 chains of human skin collagen.	COL1A1 COL1A2	5.80e-07	2	27	2	5529814
Pubmed	Comparing Clinical and Genetic Characteristics of De Novo and Inherited COL1A1/COL1A2 Variants in a Large Chinese Cohort of Osteogenesis Imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	35909573
Pubmed	Alternative splice form of type II procollagen mRNA (IIA) is predominant in skeletal precursors and non-cartilaginous tissues during early mouse development.	COL2A1 COL1A1	5.80e-07	2	27	2	8204907
Pubmed	Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	27519266
Pubmed	Biochemical markers of bone turnover and clinical outcomes in men with prostate cancer.	COL1A1 COL1A2	5.80e-07	2	27	2	21163673
Pubmed	Mutation of the 5'-untranslated region stem-loop structure inhibits α1(I) collagen expression in vivo.	COL1A1 COL1A2	5.80e-07	2	27	2	21193410
Pubmed	Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null-allele mutations.	COL1A1 COL1A2	5.80e-07	2	27	2	9443882
Pubmed	COL1A1 and COL1A2 sequencing results in cohort of patients undergoing evaluation for potential child abuse.	COL1A1 COL1A2	5.80e-07	2	27	2	27090748
Pubmed	Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients.	COL1A1 COL1A2	5.80e-07	2	27	2	15241796
Pubmed	Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogenesis imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	24668929
Pubmed	Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	36140746
Pubmed	Low density lipoproteins bind more to type I and III collagens by negative charge-dependent mechanisms than to type IV and V collagens.	COL1A1 COL1A2	5.80e-07	2	27	2	7945553
Pubmed	Relationship between genotype and skeletal phenotype in children and adolescents with osteogenesis imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	19929435
Pubmed	[Relationship of collagen type I alpha 1 and alpha 2 gene polymorphisms with bone mineral density].	COL1A1 COL1A2	5.80e-07	2	27	2	16864092
Pubmed	Cloning, characterization, and functional studies of a nonintegrin platelet receptor for type I collagen.	COL1A1 COL1A2	5.80e-07	2	27	2	9239397
Pubmed	Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxis.	COL1A1 COL1A2	5.80e-07	2	27	2	1303238
Pubmed	Assignment of the genes for mouse type I procollagen to chromosome 16 using mouse fibroblast-Chinese hamster somatic cell hybrids.	COL1A1 COL1A2	5.80e-07	2	27	2	6857446
Pubmed	Genotype-phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I.	COL1A1 COL1A2	5.80e-07	2	27	2	20087402
Pubmed	Adhesion of human neuroblasts to HIV-1 tat.	COL1A1 COL1A2	5.80e-07	2	27	2	8552450
Pubmed	Confirmation of a G nucleotide deletion in the Cola-2 gene of mice with the osteogenesis imperfecta mutation.	COL2A1 COL1A2	5.80e-07	2	27	2	8020944
Pubmed	Responsiveness to pamidronate treatment is not related to the genotype of type I collagen in patients with osteogenesis imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	28528406
Pubmed	Clinical significance and biological role of cancer-derived Type I collagen in lung and esophageal cancers.	COL1A1 COL1A2	5.80e-07	2	27	2	30604926
Pubmed	Early type I collagen deposition is associated with prognosis in biliary atresia.	COL1A1 COL1A2	5.80e-07	2	27	2	26452701
Pubmed	Homology-mediated recombination between type I collagen gene exons results in an internal tandem duplication and lethal osteogenesis imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	8097422
Pubmed	[Analysis of gross deletions of COL1A1/2 genes in Chinese families affected with osteogenesis imperfecta].	COL1A1 COL1A2	5.80e-07	2	27	2	27454992
Pubmed	Regional chromosome mapping of human collagen genes alpha 2(I) and alpha 1(I) (COLIA2 and COLIA1).	COL1A1 COL1A2	5.80e-07	2	27	2	3857213
Pubmed	No evidence for disturbed COL1A1 and A2 expression in otosclerosis.	COL1A1 COL1A2	5.80e-07	2	27	2	22130917
Pubmed	Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants.	COL1A1 COL1A2	5.80e-07	2	27	2	34902613
Pubmed	Substitutions for glycine alpha 1-637 and glycine alpha 2-694 of type I procollagen in lethal osteogenesis imperfecta. The conformational strain on the triple helix introduced by a glycine substitution can be transmitted along the helix.	COL1A1 COL1A2	5.80e-07	2	27	2	1874719
Pubmed	Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects.	COL1A1 COL1A2	5.80e-07	2	27	2	35044492
Pubmed	Differential unfolding of alpha1 and alpha2 chains in type I collagen and collagenolysis.	COL1A1 COL1A2	5.80e-07	2	27	2	18644377
Pubmed	COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta.	COL1A1 COL1A2	5.80e-07	2	27	2	21344539
Pubmed	Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study.	COL1A1 COL1A2	5.80e-07	2	27	2	31876392
Pubmed	Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome.	COL1A1 COL1A2	5.80e-07	2	27	2	23692737
Interaction	TGFBI interactions	COL2A1 COL1A1 COL1A2	4.30e-06	25	26	3	int:TGFBI
Interaction	BGN interactions	COL2A1 COL1A1 COL1A2	7.56e-06	30	26	3	int:BGN
Interaction	PDGFA interactions	COL2A1 COL1A1 COL1A2	9.22e-06	32	26	3	int:PDGFA
Interaction	SPARC interactions	COL2A1 COL1A1 COL1A2	7.90e-05	65	26	3	int:SPARC
Interaction	NEK8 interactions	ADAMTSL4 ANKS3 INVS	8.64e-05	67	26	3	int:NEK8
Interaction	MMP9 interactions	COL2A1 COL1A1 COL1A2	8.64e-05	67	26	3	int:MMP9
Interaction	COL9A1 interactions	COL2A1 PPP1R12C	1.24e-04	13	26	2	int:COL9A1
Interaction	TMEM44 interactions	COL1A1 COL1A2	1.66e-04	15	26	2	int:TMEM44
Interaction	MMP2 interactions	COL2A1 COL1A1 COL1A2	1.88e-04	87	26	3	int:MMP2
Interaction	FGF7 interactions	COL2A1 COL1A1	1.90e-04	16	26	2	int:FGF7
Interaction	PDGFB interactions	COL2A1 COL1A1 COL1A2	1.95e-04	88	26	3	int:PDGFB
Interaction	RNF144A interactions	ZDHHC18 COL1A1 COL1A2	2.15e-04	91	26	3	int:RNF144A
Interaction	CBLL2 interactions	COL1A1 COL1A2	3.00e-04	20	26	2	int:CBLL2
Cytoband	Xq13.1	RPS26P11 NALF2	3.69e-04	48	27	2	Xq13.1
GeneFamily	Collagens	COL2A1 COL1A1 COL1A2	1.02e-05	46	17	3	490
GeneFamily	Ankyrin repeat domain containing	ANKS3 PPP1R12C INVS	1.40e-03	242	17	3	403
GeneFamily	Sterile alpha motif domain containing	SAMHD1 ANKS3	3.04e-03	88	17	2	760
Coexpression	NABA_MATRISOME_PRIMARY_METASTATIC_LUNG_TUMOR	COL2A1 COL1A1 COL1A2	6.24e-06	35	27	3	MM17054
Coexpression	NABA_COLLAGENS	COL2A1 COL1A1 COL1A2	1.17e-05	43	27	3	MM17060
Coexpression	NABA_COLLAGENS	COL2A1 COL1A1 COL1A2	1.26e-05	44	27	3	M3005
Coexpression	GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_DN	COL2A1 TRIOBP RRP7A CHD7	4.65e-05	196	27	4	M10002
Coexpression	TURASHVILI_BREAST_DUCTAL_CARCINOMA_VS_LOBULAR_NORMAL_UP	GLCCI1 COL1A1 COL1A2	6.02e-05	74	27	3	M4479
Coexpression	TURASHVILI_BREAST_LOBULAR_CARCINOMA_VS_LOBULAR_NORMAL_DN	INVS COL1A1 COL1A2	6.02e-05	74	27	3	M13547
Coexpression	DESCARTES_FETAL_EYE_STROMAL_CELLS	ADAMTSL4 COL1A1 COL1A2	1.11e-04	91	27	3	M40180
Coexpression	GAO_LARGE_INTESTINE_24W_C1_DCLK1POS_PROGENITOR	ZNF469 COL1A1 COL1A2	1.43e-04	99	27	3	M39152
Coexpression	THUM_MIR21_TARGETS_HEART_DISEASE_UP	COL1A1 COL1A2	1.55e-04	18	27	2	M13796
Coexpression	KANG_AR_TARGETS_DN	COL1A1 COL1A2	1.55e-04	18	27	2	M2225
Coexpression	THUM_MIR21_TARGETS_HEART_DISEASE_UP	COL1A1 COL1A2	1.55e-04	18	27	2	MM1241
Coexpression	KANG_AR_TARGETS_DN	COL1A1 COL1A2	1.55e-04	18	27	2	MM892
Coexpression	LIAO_METASTASIS	RRP7A CHD7 RCC2 COL1A1 COL1A2	2.02e-04	540	27	5	M13809
Coexpression	DESCARTES_MAIN_FETAL_STROMAL_CELLS	COL1A1 COL1A2	2.33e-04	22	27	2	M40074
Coexpression	SCHLINGEMANN_SKIN_CARCINOGENESIS_TPA_DN	COL1A1 COL1A2	3.27e-04	26	27	2	M1623
Coexpression	SCHLINGEMANN_SKIN_CARCINOGENESIS_TPA_DN	COL1A1 COL1A2	3.27e-04	26	27	2	MM1193
Coexpression	DESCARTES_FETAL_THYMUS_STROMAL_CELLS	ADAMTSL4 COL1A1 COL1A2	3.73e-04	137	27	3	M40313
Coexpression	CHIARADONNA_NEOPLASTIC_TRANSFORMATION_KRAS_DN	SAMHD1 COL1A1 COL1A2	4.05e-04	141	27	3	M10381
Coexpression	NABA_MATRISOME_METASTATIC_LUNG_LYMPH_NODE_METASTASIS	COL2A1 COL1A1	4.08e-04	29	27	2	MM17055
Coexpression	NAKAMURA_CANCER_MICROENVIRONMENT_UP	COL1A1 COL1A2	4.08e-04	29	27	2	M7581
Coexpression	CHIARADONNA_NEOPLASTIC_TRANSFORMATION_KRAS_DN	SAMHD1 COL1A1 COL1A2	4.49e-04	146	27	3	MM973
Coexpression	DESCARTES_FETAL_KIDNEY_STROMAL_CELLS	ADAMTSL4 COL1A1 COL1A2	4.49e-04	146	27	3	M40222
Coexpression	DESCARTES_FETAL_HEART_STROMAL_CELLS	COL1A1 COL1A2	5.62e-04	34	27	2	M40199
Coexpression	HATADA_METHYLATED_IN_LUNG_CANCER_UP	COL2A1 ADAMTSL4 COL1A1 COL1A2	5.69e-04	377	27	4	M19508
Coexpression	MURARO_PANCREAS_MESENCHYMAL_STROMAL_CELL	ZNF469 ANO6 RCC2 COL1A1 COL1A2	5.86e-04	681	27	5	M39175
Coexpression	CARRILLOREIXACH_HEPATOBLASTOMA_VS_NORMAL_HYPOMETHYLATED_AND_UP	COL2A1 COL1A1 COL1A2	6.08e-04	162	27	3	M45037
Coexpression	GSE40274_CTRL_VS_HELIOS_TRANSDUCED_ACTIVATED_CD4_TCELL_UP	RIPOR2 ANO6 INVS	6.53e-04	166	27	3	M9100
Coexpression	GSE40274_CTRL_VS_FOXP3_AND_EOS_TRANSDUCED_ACTIVATED_CD4_TCELL_UP	SAMHD1 RIPOR2 ANO6	6.87e-04	169	27	3	M9102
Coexpression	LEE_AGING_MUSCLE_DN	COL1A1 COL1A2	7.78e-04	40	27	2	M1574
Coexpression	GSE18791_UNSTIM_VS_NEWCATSLE_VIRUS_DC_18H_DN	RIPOR2 GLCCI1 NSUN7	9.94e-04	192	27	3	M4296
Coexpression	GSE18791_CTRL_VS_NEWCASTLE_VIRUS_DC_18H_DN	RIPOR2 GLCCI1 NSUN7	1.01e-03	193	27	3	M4284
Coexpression	GSE13485_DAY3_VS_DAY21_YF17D_VACCINE_PBMC_UP	KIF13A RCC2 INVS	1.01e-03	193	27	3	M3303
Coexpression	GSE29618_BCELL_VS_MDC_UP	CHD7 RIPOR2 CR1	1.02e-03	194	27	3	M4943
Coexpression	JONES_OVARY_THECA	COL1A1 COL1A2	1.03e-03	46	27	2	M48349
Coexpression	LEE_AGING_MUSCLE_DN	COL1A1 COL1A2	1.03e-03	46	27	2	MM670
Coexpression	KHETCHOUMIAN_TRIM24_TARGETS_UP	COL1A1 COL1A2	1.03e-03	46	27	2	MM544
Coexpression	KHETCHOUMIAN_TRIM24_TARGETS_UP	COL1A1 COL1A2	1.07e-03	47	27	2	M1399
Coexpression	TURASHVILI_BREAST_DUCTAL_CARCINOMA_VS_DUCTAL_NORMAL_UP	COL1A1 COL1A2	1.07e-03	47	27	2	M7585
Coexpression	GSE3982_BCELL_VS_CENT_MEMORY_CD4_TCELL_DN	ZDHHC18 SAMHD1 TTLL3	1.09e-03	198	27	3	M5545
Coexpression	HAY_BONE_MARROW_NEUTROPHIL	TRIOBP CR1 KIF13A ANO6	1.10e-03	450	27	4	M39203
Coexpression	GSE26351_WNT_VS_BMP_PATHWAY_STIM_HEMATOPOIETIC_PROGENITORS_UP	TRIOBP SAMHD1 COL1A2	1.10e-03	199	27	3	M8477
Coexpression	GSE6674_ANTI_IGM_VS_ANTI_IGM_AND_CPG_STIM_BCELL_UP	SAMHD1 RIPOR2 GLCCI1	1.10e-03	199	27	3	M6934
Coexpression	GSE22432_MULTIPOTENT_VS_COMMON_DC_PROGENITOR_UP	KIF13A RCC2 CEP170B	1.10e-03	199	27	3	M7821
Coexpression	GSE3691_CONVENTIONAL_VS_PLASMACYTOID_DC_SPLEEN_UP	RIPOR2 ADAMTSL4 GLCCI1	1.12e-03	200	27	3	M6369
Coexpression	GSE41867_DAY6_EFFECTOR_VS_DAY30_MEMORY_CD8_TCELL_LCMV_ARMSTRONG_DN	CHD7 TTLL3 ANKS3	1.12e-03	200	27	3	M9459
Coexpression	GSE3039_CD4_TCELL_VS_B2_BCELL_UP	TRIOBP GLCCI1 ANKS3	1.12e-03	200	27	3	M6462
Coexpression	GSE29164_UNTREATED_VS_CD8_TCELL_TREATED_MELANOMA_DAY7_DN	THSD7B KIAA1614 CEP170B	1.12e-03	200	27	3	M8496
Coexpression	GSE22886_NAIVE_CD4_TCELL_VS_48H_ACT_TH2_UP	SAMHD1 CHD7 RIPOR2	1.12e-03	200	27	3	M4528
Coexpression	GSE27786_BCELL_VS_NKCELL_UP	RIPOR2 RCC2 CEP170B	1.12e-03	200	27	3	M4805
Coexpression	GSE36078_WT_VS_IL1R_KO_LUNG_DC_AFTER_AD5_T425A_HEXON_INF_UP	SAMHD1 CHD7 TTLL3	1.12e-03	200	27	3	M9294
Coexpression	GSE36078_UNTREATED_VS_AD5_INF_IL1R_KO_MOUSE_LUNG_DC_DN	TRIOBP CHD7 TTLL3	1.12e-03	200	27	3	M9296
Coexpression	GSE15330_WT_VS_IKAROS_KO_HSC_UP	SAMHD1 CHD7 TTLL3	1.12e-03	200	27	3	M7040
Coexpression	CUI_DEVELOPING_HEART_SMOOTH_MUSCLE_CELL	COL1A1 COL1A2	1.12e-03	48	27	2	M39318
ToppCell	PCW_13-14-Mesenchymal-Mesenchymal_fibroblastic-mes_adventitial_fibro_(10)\|PCW_13-14 / Celltypes from embryonic and fetal-stage human lung	ZNF469 ADAMTSL4 COL1A1 COL1A2	5.33e-06	193	27	4	adc9fc94f9ec686a417d08c0b8b7b7ab687afec0
ToppCell	15-Trachea-Mesenchymal\|Trachea / Age, Tissue, Lineage and Cell class	THSD7B ADAMTSL4 COL1A1 COL1A2	5.67e-06	196	27	4	7e178c76285e61c721c38d7a995ebf89dc428f9f
ToppCell	15-Trachea-Mesenchymal-Mesenchyme_SERPINF1-high\|Trachea / Age, Tissue, Lineage and Cell class	THSD7B ADAMTSL4 COL1A1 COL1A2	5.67e-06	196	27	4	54aefcebf13704f51de84379e2e22ec0734b9461
ToppCell	Parenchymal-10x3prime_v2-Stromal-Mesofibroblastic\|10x3prime_v2 / Cell types per location group and 10X technology with lineage, and cell group designations	ZNF469 THSD7B COL1A1 COL1A2	5.90e-06	198	27	4	0cd930e374c2c48d1991b51c025f9801b22ecee7
ToppCell	Parenchymal-10x3prime_v2-Stromal-Mesofibroblastic-Mesothelia\|10x3prime_v2 / Cell types per location group and 10X technology with lineage, and cell group designations	ZNF469 THSD7B COL1A1 COL1A2	5.90e-06	198	27	4	e0df6d6ff2a9c41d813f84a2a5ee7cb5f6fc3e30
ToppCell	3'-Adult-LargeIntestine-Mesenchymal-fibroblastic\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	SAMHD1 ADAMTSL4 COL1A1 COL1A2	6.14e-06	200	27	4	cbf6a6c3db88bac37bd084a3a914b12b3af524eb
ToppCell	P28-Mesenchymal-mesenchymal_fibroblast-mesenchymal_progenitor_cell\|P28 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase	NSUN7 COL1A1 COL1A2	1.08e-04	154	27	3	44d4d99b08216c0901e3bc32743fa0a8b85b5149
ToppCell	Influenza_Severe-Neutrophil\|Influenza_Severe / Disease group and Cell class	ZDHHC18 RIPOR2 NSUN7	1.24e-04	161	27	3	98c95b1b85d5427415af2ca8fb14849e97f6e8b5
ToppCell	343B-Fibroblasts-Fibroblast-D-\|343B / Donor, Lineage, Cell class and subclass (all cells)	KIAA1614 COL1A1 COL1A2	1.28e-04	163	27	3	8d2b2119c6b3d5b677da6f377fd85146590e1246
ToppCell	343B-Fibroblasts-Fibroblast-D\|343B / Donor, Lineage, Cell class and subclass (all cells)	KIAA1614 COL1A1 COL1A2	1.28e-04	163	27	3	acfb2ece6202479e615d54fd3ecb8b4a571b5a18
ToppCell	normal_Lung-Fibroblasts-Myofibroblasts\|Fibroblasts / Location, Cell class and cell subclass	ZNF469 COL1A1 COL1A2	1.30e-04	164	27	3	9b4a6007abae992db871d9f6f731d5af724de30d
ToppCell	Children_(3_yrs)-Mesenchymal-airway_smooth_muscle_cell-D046\|Children_(3_yrs) / Lineage, Cell type, age group and donor	THSD7B COL1A1 COL1A2	1.30e-04	164	27	3	e3983f655cdba308fb192182829f17bef99ce0ba
ToppCell	facs-Limb_Muscle-forelimb_and_hindlimb-18m-Mesenchymal-mesenchymal_stem_cell\|Limb_Muscle / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation	COL2A1 COL1A1 COL1A2	1.33e-04	165	27	3	f80665b75d43f1bf6919d59fc762e7e0bac653f2
ToppCell	renal_medulla_nuclei-Hypertensive_with+without-CKD-Immune-Myeloid-Granulocytic-Neutrophil\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	ZDHHC18 RIPOR2 CR1	1.35e-04	166	27	3	6a65dff1333f39ec8c584e6df04b8c1e7f1c8946
ToppCell	TCGA-Lung-Primary_Tumor-Lung_Carcinoma-Lung_Squamous_Cell_Carcinoma-4\|TCGA-Lung / Sample_Type by Project: Shred V9	ZNF469 COL1A1 COL1A2	1.40e-04	168	27	3	aefea14b8b1c1b6a05f827effd22ba15274fddc9
ToppCell	Hippocampus-Endothelial-ENDOTHELIAL_TIP\|Hippocampus / BrainAtlas - Mouse McCarroll V32	ADAMTSL4 COL1A1 COL1A2	1.40e-04	168	27	3	26aa96b2b547d11941cb803995ea3d302ee0518c
ToppCell	E18.5-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF1-AF1_prolif\|E18.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	KIAA1614 ANKS3 COL1A2	1.43e-04	169	27	3	16c52a0f6d96ecc1832922fce9b39691849f0d73
ToppCell	5'-Adult-LargeIntestine-Mesenchymal-fibroblastic-Stromal_1_(ADAMDEC1+)\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	SAMHD1 COL1A1 COL1A2	1.43e-04	169	27	3	c0824a93674e2bff0f09b2d2fab5bab016a2e379
ToppCell	PND10-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2-AF2_mature\|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	ZNF469 COL1A1 COL1A2	1.43e-04	169	27	3	031465190cd3623a25ef2b868daab8d932c8ff08
ToppCell	renal_medulla_nuclei-Adult_normal_reference-Mesenchymal-Fibroblast-kidney_interstitial_fibroblast\|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group	SAMHD1 COL1A1 COL1A2	1.48e-04	171	27	3	5d31fc9b60329d4ae3c77e4ca679359d9314397d
ToppCell	saliva-Severe-critical_progression_d12-22_with-steroid-Myeloid-Granulocytic\|Severe-critical_progression_d12-22_with-steroid / Compartment, severity and other cell annotations on 10x 3' data (130k)	ZDHHC18 RIPOR2 ADAMTSL4	1.48e-04	171	27	3	2b7c5a557c4bc5c573211c4d618bdd6766a24916
ToppCell	PND10-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2\|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	ZNF469 COL1A1 COL1A2	1.48e-04	171	27	3	15cb4670ff4234ac46aea8a5911138d6913c4482
ToppCell	saliva-Severe-critical_progression_d12-22_with-steroid-Myeloid-Granulocytic-Neutrophil\|Severe-critical_progression_d12-22_with-steroid / Compartment, severity and other cell annotations on 10x 3' data (130k)	ZDHHC18 RIPOR2 ADAMTSL4	1.48e-04	171	27	3	dcb15bc54aeea06ef8f07f1134f3ff1e21ac0e4f
ToppCell	renal_cortex_nuclei-Renal_AKI_(acute_kidney_injury)-Immune-Myeloid-Granulocytic-Neutrophil\|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group	ZDHHC18 RIPOR2 CR1	1.53e-04	173	27	3	dfa56753319c92ae5b337793c4d6d5f70afce546
ToppCell	3'-Child09-12-SmallIntestine-Mesenchymal-fibroblastic-Stromal_3_(C7+)\|Child09-12 / Celltypes from developing, pediatric, Crohn's, & adult GI tract	ADAMTSL4 COL1A1 COL1A2	1.53e-04	173	27	3	11e95a60b5f6f07f27154a23203bac431e7528c6
ToppCell	3'-GW_trimst-2-LargeIntestine-Mesenchymal-fibroblastic-Stromal_3_(KCNN3+)\|GW_trimst-2 / Celltypes from developing, pediatric, Crohn's, & adult GI tract	GLCCI1 COL1A1 COL1A2	1.55e-04	174	27	3	9d22a554617a93701d0945de63cc3e7b24322c40
ToppCell	CF-Myeloid-Neutrophil\|Myeloid / Disease state, Lineage and Cell class	ZDHHC18 RIPOR2 CR1	1.58e-04	175	27	3	8020c3a34f77e68e8149f87481fb1dddd2ac675e
ToppCell	PND07-28-samps-Mesenchymal-Myofibroblast-myofibroblast_-_mature_-_DCN\|PND07-28-samps / Age Group, Lineage, Cell class and subclass	ADAMTSL4 COL1A1 COL1A2	1.61e-04	176	27	3	08f94b78b27feeb113dbfadbfa7fe34d08b2809b
ToppCell	renal_medulla_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Myocytic_interstitial_cell-Vascular_Smooth_Muscle_Cell_/_Pericyte-\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	THSD7B COL1A1 COL1A2	1.63e-04	177	27	3	4943d040eee0f9dceaddc7498171281d170e271f
ToppCell	renal_medulla_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Myocytic_interstitial_cell-Vascular_Smooth_Muscle_Cell_/_Pericyte\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	THSD7B COL1A1 COL1A2	1.63e-04	177	27	3	3f2272b577c862dba8ccfb41184054bbd0ace6f5
ToppCell	3'-GW_trimst-1.5-LargeIntestine-Mesenchymal-fibroblastic-Stromal_3_(C7+)\|GW_trimst-1.5 / Celltypes from developing, pediatric, Crohn's, & adult GI tract	ADAMTSL4 COL1A1 COL1A2	1.63e-04	177	27	3	7af1a19692f7fe8f691178a4e57d62bc379e3d56
ToppCell	metastatic_Brain-T/NK_cells-Exhausted_Tfh\|T/NK_cells / Location, Cell class and cell subclass	RCC2 CEP170B PPP1R12C	1.66e-04	178	27	3	9a3581a0158dfa5a1cc942f8c532afb5e38b272a
ToppCell	TCGA-Ovary-Primary_Tumor-Ovarian_Carcinoma-Serous_Cystadenocarcinoma-6\|TCGA-Ovary / Sample_Type by Project: Shred V9	ZNF469 COL1A1 COL1A2	1.66e-04	178	27	3	142879e9393e721f9b05a6bb46995c9d6d713c95
ToppCell	TCGA-Colorectal-Primary_Tumor-Colorectal_Adenocarcinoma-Mucinous_Colon_Adenocarcinoma-10\|TCGA-Colorectal / Sample_Type by Project: Shred V9	ZNF469 RIPOR2 CR1	1.69e-04	179	27	3	cc079ba015326dccde955c5eafa3e4a2e40de192
ToppCell	Brain_organoid-organoid_Kanton_Nature-Organoid-4M-Neuronal-ventral_progenitors_and_neurons_2\|Organoid-4M / Sample Type, Dataset, Time_group, and Cell type.	CHD7 GLCCI1 COL1A2	1.69e-04	179	27	3	d95367d689732ab2653e8d70d8d8e5eb15ae6eef
ToppCell	PND10-Mesenchymal-Mesenchymal_myocytic-Myofibroblast_airway-SCMF-SCMF_prolif\|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	COL2A1 COL1A1 COL1A2	1.69e-04	179	27	3	ff678e2f33c914e3dd0f338ada25f506c3e3c980
ToppCell	5'-Airway_Nasal-Mesenchymal-Fibroblastic\|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5	ZNF469 COL1A1 COL1A2	1.72e-04	180	27	3	935c091bbcd6d10b81dc4731779e5bd98205c99f
ToppCell	5'-Airway_Nasal-Mesenchymal\|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5	ZNF469 COL1A1 COL1A2	1.72e-04	180	27	3	3dd384b7f3d9582b8fec9fe05100e466e6218b76
ToppCell	Control-Fibroblasts-Airway_smooth_muscle\|Control / group, cell type (main and fine annotations)	THSD7B COL1A1 COL1A2	1.72e-04	180	27	3	d0de12749ef0f51f0931c6e7b9b99966bdbc3ec1
ToppCell	PND14-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2-AF2_mature\|PND14 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	ZNF469 COL1A1 COL1A2	1.74e-04	181	27	3	6730e249cac55ae892cc567d9211615882f3dab4
ToppCell	PND14-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2\|PND14 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	ZNF469 COL1A1 COL1A2	1.74e-04	181	27	3	3462aa1c08fbaf613b6278ab2c7a5a0940bf537d
ToppCell	P15-Mesenchymal-mesenchymal_fibroblast-mesenchymal_alveolar_niche_cell\|P15 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase	ZNF469 COL1A1 COL1A2	1.77e-04	182	27	3	e9fcae9d03a6faf85b91882c5da699037bc61aeb
ToppCell	facs-Brain_Non-Myeloid-Cerebellum_-18m-Epithelial-nan\|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation	TTLL3 COL1A1 COL1A2	1.77e-04	182	27	3	904804813849b7f7f716ba1554d33b07bc0a701e
ToppCell	renal_medulla_nuclei-Adult_normal_reference-Mesenchymal-Fibroblast-Collagen+matrisome-high_fibroblast\|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group	SAMHD1 COL1A1 COL1A2	1.77e-04	182	27	3	44764676ed3f51ba171ce63f669390392fa50a43
ToppCell	saliva-Severe-critical_progression_d12-22_with-steroid-Myeloid-Granulocytic-Neutrophil-Neu_c1-IL1B\|Severe-critical_progression_d12-22_with-steroid / Compartment, severity and other cell annotations on 10x 3' data (130k)	ZDHHC18 RIPOR2 ADAMTSL4	1.77e-04	182	27	3	dc32f8f6a3b13918eb8e93c018f5823d86344080
ToppCell	facs-Brain_Non-Myeloid-Cerebellum_-18m-Epithelial\|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation	TTLL3 COL1A1 COL1A2	1.77e-04	182	27	3	5d8b7fe18286e27f0f50c5d2d9be56850e2cb8f4
ToppCell	renal_medulla_nuclei-Adult_normal_reference-Mesenchymal-Fibroblast-Collagen+matrisome-high_fibroblast-\|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group	SAMHD1 COL1A1 COL1A2	1.77e-04	182	27	3	d82f59a3f930a840dde27dc6ab024f227a26d446
ToppCell	TCGA-Thryoid-Primary_Tumor-Thyroid_Papillary_Carcinoma-Classical-1\|TCGA-Thryoid / Sample_Type by Project: Shred V9	ZNF469 COL1A1 COL1A2	1.80e-04	183	27	3	06e4b05d86a7d643569e19575c2c9aa351d33f29
ToppCell	10x_3'_v2v3-Neoplastic-Stem-like-NPC-like-NPC-like_neural-A\|10x_3'_v2v3 / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group	CHD7 GLCCI1 COL1A2	1.80e-04	183	27	3	af14da45267261e775dd6dab7a4c359b181e46f1
ToppCell	5'-Airway_Nasal-Mesenchymal-Fibroblastic-fibroblastic_type_2-Peribronchial_fibroblasts-Peribronchial_fibroblasts_L.2.1.3.1\|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5	ZNF469 COL1A1 COL1A2	1.80e-04	183	27	3	6d98973098c6d20c5305bce6a83a549a7d8dbfba
ToppCell	5'-Airway_Nasal-Mesenchymal-Fibroblastic-fibroblastic_type_2-Peribronchial_fibroblasts\|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5	ZNF469 COL1A1 COL1A2	1.80e-04	183	27	3	cc7f5a17b40e8d901885174922e5fa8877643071
ToppCell	Mesenchymal_cells-Osteoblasts\|Mesenchymal_cells / Lineage and Cell class	ZNF469 COL1A1 COL1A2	1.80e-04	183	27	3	d6b52d52fe9a7a6c798947f05420d79fe12e4662
ToppCell	5'-Airway_Nasal-Mesenchymal-Fibroblastic-fibroblastic_type_2\|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5	ZNF469 COL1A1 COL1A2	1.80e-04	183	27	3	803376f5260de83c48d4f7301278d078a32b3e6e
ToppCell	P07-Mesenchymal-mesenchymal_fibroblast-mesenchymal_alveolar_niche_cell\|P07 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase	ZNF469 COL1A1 COL1A2	1.83e-04	184	27	3	01257e5c12e38b849fd3d9496c43ded666249ba5
ToppCell	normal_Lung-Fibroblasts-Myofibroblasts\|normal_Lung / Location, Cell class and cell subclass	ZNF469 COL1A1 COL1A2	1.83e-04	184	27	3	0b336489c10e8c3c957795dd845454f03404382b
ToppCell	mild-Myeloid-mDC\|mild / Cohort 2 (Rhapsody WB + PBMC) with disease condition, lineage and cell classs	ZNF469 SAMHD1 RCC2	1.83e-04	184	27	3	8b37c00d59d9992d3b43268991da7bb94646c70e
ToppCell	Smart-seq2-tissue-resident_(Smart-seq2)-myeloid-myeloid_granulocytic-neutrophil\|tissue-resident_(Smart-seq2) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type	ZDHHC18 RIPOR2 CR1	1.83e-04	184	27	3	7ecdf2645e9378cf2f5ce4557f2cf100e6f184ba
ToppCell	primary_auditory_cortex_(A1C)-Non-neuronal-Macroglial-Oligo-OPC-OPC_L1-6_MYT1\|primary_auditory_cortex_(A1C) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types	CHD7 KIF13A NSUN7	1.86e-04	185	27	3	efc5d564f8793c751ba640aef60f761e4b081d3f
ToppCell	PCW_13-14-Mesenchymal-Mesenchymal_fibroblastic-mes_Arw_fibro_(16)\|PCW_13-14 / Celltypes from embryonic and fetal-stage human lung	ADAMTSL4 COL1A1 COL1A2	1.86e-04	185	27	3	7dcdc009c5681ee05dd18968f7e85c3403fe34af
ToppCell	primary_auditory_cortex_(A1C)-Non-neuronal-Macroglial-Oligo-OPC\|primary_auditory_cortex_(A1C) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types	CHD7 KIF13A NSUN7	1.86e-04	185	27	3	fba2dc46cd98ab9c78e788959c2121aa10d148b2
ToppCell	390C-Fibroblasts-Fibroblast-F\|390C / Donor, Lineage, Cell class and subclass (all cells)	ADAMTSL4 COL1A1 COL1A2	1.86e-04	185	27	3	2c1f14f77faeee2acb388d997c5a27a7fef79be1
ToppCell	390C-Fibroblasts-Fibroblast-F-\|390C / Donor, Lineage, Cell class and subclass (all cells)	ADAMTSL4 COL1A1 COL1A2	1.86e-04	185	27	3	37db8e0b1f59274227f6fc2362167eb44bd080ef
ToppCell	Influenza-Influenza_Severe-Myeloid-Neutrophil\|Influenza_Severe / Disease, condition lineage and cell class	ZDHHC18 CR1 NSUN7	1.89e-04	186	27	3	1dfcec9196d4db76fba3abc74e85885b1fb98b87
ToppCell	3'-Adult-LargeIntestine-Mesenchymal-fibroblastic-Stromal_1_(ADAMDEC1+)\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	ADAMTSL4 COL1A1 COL1A2	1.92e-04	187	27	3	6f47a80e612b320f571210483e62ff5db2a8ea43
ToppCell	3'-Adult-LargeIntestine-Mesenchymal-stromal_related-T_reticular\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	ADAMTSL4 COL1A1 COL1A2	1.92e-04	187	27	3	f0c4d93f75615e570e4465fd622e3124189618a1
ToppCell	LA-01._Fibroblast_I\|World / Chamber and Cluster_Paper	ADAMTSL4 COL1A1 COL1A2	1.92e-04	187	27	3	4ea486991f66c29728d127171a07b81404ec0b78
ToppCell	3'-Adult-LargeIntestine-Mesenchymal-stromal_related\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	ADAMTSL4 COL1A1 COL1A2	1.92e-04	187	27	3	3ff57da09ed8394913fb683669d7bff84a936623
ToppCell	PCW_07-8.5-Mesenchymal-Mesenchymal_fibroblastic-mes_immature3_(17)\|PCW_07-8.5 / Celltypes from embryonic and fetal-stage human lung	ANO6 COL1A1 COL1A2	1.92e-04	187	27	3	a9316e2818217ec5feae9cf8816f7249803caee6
ToppCell	Mesenchymal-chondrocyte\|World / Lineage, Cell type, age group and donor	COL2A1 COL1A1 COL1A2	1.95e-04	188	27	3	7b1e3f8a941eaa68e89c562129a92314642eec66
ToppCell	PBMC-Severe-Myeloid-Neutrophil-Neutrophil-Neu_1\|Severe / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)	ZDHHC18 RIPOR2 CR1	1.95e-04	188	27	3	aa46073e2940dc1d2020b2e259bf0fc06cb990ee
ToppCell	(2)_Fibroblasts-(20)_Fibro-1\|World / Cell class and subclass of bone marrow stroma cells in homeostatis	ADAMTSL4 COL1A1 COL1A2	1.95e-04	188	27	3	409a7b69d02e87084ca955e3fe6c77230dee8861
ToppCell	PBMC-Severe-Myeloid-Neutrophil-Neutrophil-Neu_1\|Severe / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)	ZDHHC18 RIPOR2 CR1	1.95e-04	188	27	3	04814b78da936a51a497e23060d19ca0d619e250
ToppCell	Mesenchymal_cells-Osteoblasts\|World / Lineage and Cell class	ZNF469 COL1A1 COL1A2	1.95e-04	188	27	3	89f7f5a51be7e046a63e2413f86c521ae4b6718f
ToppCell	10x5'v1-week_14-16-Mesenchymal_fibro-stroma\|week_14-16 / cell types per 3 fetal stages;per 3',per 5'	COL2A1 COL1A1 COL1A2	1.98e-04	189	27	3	eccf3d49354a67c94f1ed7c15a98a48a5e8e2ed0
ToppCell	10x_3'_v3-spleen_(10x_3'_v3)\|10x_3'_v3 / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type	ZDHHC18 RIPOR2 CR1	1.98e-04	189	27	3	0fe8901e10c619c93b7788792da1706a32102c6e
ToppCell	10x5'v1-week_14-16-Mesenchymal_fibro\|week_14-16 / cell types per 3 fetal stages;per 3',per 5'	COL2A1 COL1A1 COL1A2	1.98e-04	189	27	3	40764f461b8aa1d3a2c5a30590b7fb9307d47d09
ToppCell	Mesenchymal-airway_smooth_muscle_cell\|World / Lineage, Cell type, age group and donor	THSD7B COL1A1 COL1A2	2.01e-04	190	27	3	645e56b02edc3702c7db917b8ecd5eed0decaf71
ToppCell	PCW_10-12-Mesenchymal-Mesenchymal_fibroblastic-mes_adventitial_fibro_(10)\|PCW_10-12 / Celltypes from embryonic and fetal-stage human lung	ADAMTSL4 COL1A1 COL1A2	2.01e-04	190	27	3	4f775ee24b14733f06ae40b45f2dc1a0f0df0705
ToppCell	10x5'v1-week_14-16-Myeloid_macrophage-stroma-erythroid_macrophage\|week_14-16 / cell types per 3 fetal stages;per 3',per 5'	KIAA1614 COL1A1 COL1A2	2.01e-04	190	27	3	cf463b2f227f3cc7d3fd296c810c0cbe51cbee72
ToppCell	Brain_organoid-organoid_Paulsen_bioRxiv-3.5_mon-Neuronal-Immature_INs\|3.5_mon / Sample Type, Dataset, Time_group, and Cell type.	CHD7 RIPOR2 COL1A2	2.01e-04	190	27	3	842760bfe0a52e67bad800efa7d99448a4a23ebb
ToppCell	ILEUM-non-inflamed-(8)_Activated_fibroblasts\|non-inflamed / shred on tissue, inflammation_status, cell class(v3), cell subclass (v2)	KIF13A COL1A1 COL1A2	2.01e-04	190	27	3	39fa110d19c97c7cac99f5fb91b26bc08e2f3b42
ToppCell	droplet-Lung-LUNG-1m-Mesenchymal-Myofibroblast\|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation	THSD7B COL1A1 COL1A2	2.04e-04	191	27	3	9d3fa8d8138700640cc7927521c7635299df697d
ToppCell	E18.5-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2-AF2_mature\|E18.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	ZNF469 COL1A1 COL1A2	2.04e-04	191	27	3	75d2197076a9dfc868e8baf95bd4c5e44f438e3e
ToppCell	10x5'v1-week_14-16-Mesenchymal_fibro-stroma-endosteal_fibroblast\|week_14-16 / cell types per 3 fetal stages;per 3',per 5'	COL2A1 THSD7B COL1A1	2.04e-04	191	27	3	44b1f62fdee03b157fe545f2ae6ff84f8929a8ac
ToppCell	10x5'v1-week_14-16-Mesenchymal_fibro-stroma-arteriolar_fibroblast\|week_14-16 / cell types per 3 fetal stages;per 3',per 5'	COL2A1 COL1A1 COL1A2	2.04e-04	191	27	3	5271198116343c07202649889057e5774d7fdde3
ToppCell	droplet-Lung-18m-Mesenchymal-fibroblast-adventitial_fibroblast-adventitial_fibroblast_l17\|18m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype	THSD7B COL1A1 COL1A2	2.04e-04	191	27	3	b51e0f5d1b93f526160c904e9091313a5364f3a7
ToppCell	droplet-Lung-LUNG-1m-Mesenchymal-pulmonary_interstitial_fibroblast\|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation	THSD7B COL1A1 COL1A2	2.04e-04	191	27	3	d04ed1e04b8cb904237d8e8388fe7740c724237b
ToppCell	E18.5-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2\|E18.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	ZNF469 COL1A1 COL1A2	2.04e-04	191	27	3	4b50fdd310701251e64e16cd2d07ce03dbfd3e3e
ToppCell	renal_cortex_nuclei-CKD+DKD_normotensive-Immune-Myeloid-Monocytic-Non-classical_Monocyte\|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group	SAMHD1 RIPOR2 CR1	2.04e-04	191	27	3	47a2afc4102199b4bc76bd01b2967c8016186462
ToppCell	T_cells-Central_memory_CD4+_T_cells\|T_cells / Immune cells in Kidney/Urine in Lupus Nephritis	CHD7 RIPOR2 CR1	2.04e-04	191	27	3	25dd538d6a361bd3367c8a1c0dfc9e7003061af3
ToppCell	renal_medulla_nuclei-Adult_normal_reference-Mesenchymal-Myocytic_interstitial_cell\|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group	THSD7B COL1A1 COL1A2	2.08e-04	192	27	3	24e2f15f5767a97eb3b389922bcfd7b13805e1ce
ToppCell	B_cells-Memory_B_cells\|World / Immune cells in Rheumatoid Arthritis Joint Synovial Tissues	CHD7 RIPOR2 CR1	2.08e-04	192	27	3	eef591095921ede098f41a2b81897b18915bb753
ToppCell	droplet-Lung-1m-Mesenchymal-myofibroblast\|1m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype	THSD7B COL1A1 COL1A2	2.08e-04	192	27	3	dc4b4e16e6eb212e45fb70695afd1c7e91027407
ToppCell	droplet-Lung-1m-Mesenchymal-myofibroblast-myofibroblast_cell-pulmonary_interstitial_myofibroblast\|1m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype	THSD7B COL1A1 COL1A2	2.11e-04	193	27	3	2b80991e7ba7640f7ab2139d30e4c54d8e533862
ToppCell	droplet-Heart-HEART_(ALL_MINUS_AORTA)-30m-Mesenchymal-fibroblast_of_cardiac_tissue\|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation	ADAMTSL4 COL1A1 COL1A2	2.11e-04	193	27	3	0a665531d581d4e3941e29d3f95569da8f166447
ToppCell	droplet-Lung-1m-Mesenchymal-myofibroblast-myofibroblast_cell\|1m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype	THSD7B COL1A1 COL1A2	2.11e-04	193	27	3	90cfc34c2d0d7c70f071703d35db1d6037961481
ToppCell	CF-Lymphoid-B_cell\|Lymphoid / Disease state, Lineage and Cell class	CHD7 RIPOR2 CR1	2.11e-04	193	27	3	7ebf20344a9a154fd2cffa281526867fcf0aded3
ToppCell	B_cells-Activate_B_cells\|World / Immune cells in Kidney/Urine in Lupus Nephritis	CHD7 RIPOR2 CR1	2.11e-04	193	27	3	b6da81920cf2e55f87ec8d4b2b5530cbf7ba2155
ToppCell	droplet-Heart-HEART_(ALL_MINUS_AORTA)-30m-Mesenchymal-fibroblast\|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation	ADAMTSL4 COL1A1 COL1A2	2.11e-04	193	27	3	24ce1f37cca655415410d2403a52d1ebb3332280
ToppCell	control-Myeloid-Neutrophils_3\|control / Cohort 2 (Rhapsody WB + PBMC) with disease condition, lineage and cell classs	ZDHHC18 RIPOR2 CR1	2.11e-04	193	27	3	56daf3c59a124dd068af5409113913d9ee81a454
Computational	Neighborhood of CDH11	COL1A1 COL1A2	6.11e-04	25	16	2	GNF2_CDH11
Computational	Neighborhood of PTX3	COL1A1 COL1A2	1.27e-03	36	16	2	GNF2_PTX3
Computational	Genes upregulated in subsets of cells of a given type within various tumors	COL1A1 COL1A2	2.44e-03	50	16	2	GAVISH_3CA_METAPROGRAM_FIBROBLASTS_CAF_1
Computational	Genes upregulated in subsets of cells of a given type within various tumors	CHD7 GLCCI1	2.44e-03	50	16	2	GAVISH_3CA_MALIGNANT_METAPROGRAM_29_NPC_OPC
Computational	Genes upregulated in subsets of cells of a given type within various tumors	COL1A1 COL1A2	2.44e-03	50	16	2	GAVISH_3CA_MALIGNANT_METAPROGRAM_12_EMT_1
Drug	Collagenase	COL2A1 COL1A1 COL1A2	5.94e-09	4	27	3	DB00048
Drug	ascorbate-2-phosphate	COL2A1 COL1A1 COL1A2	6.70e-07	15	27	3	ctd:C011669
Drug	5'-methylthioadenosine	COL1A1 COL1A2	1.35e-06	2	27	2	ctd:C008500
Drug	isodesmosine	COL2A1 COL1A1 COL1A2	7.92e-06	33	27	3	CID000013811
Drug	diacetylrhein	COL2A1 COL1A1	8.11e-06	4	27	2	ctd:C025292
Drug	GK-101	COL2A1 COL1A1 COL1A2	1.03e-05	36	27	3	CID000161853
Drug	BPAT-143	COL2A1 COL1A1	2.03e-05	6	27	2	CID000146249
Drug	2-phenyl-4-(3-pyridin-2-yl-1H-pyrazol-4-yl)pyridine	COL1A1 COL1A2	2.03e-05	6	27	2	ctd:C502971
Drug	AG-H-50319	COL2A1 COL1A1	2.03e-05	6	27	2	CID011819195
Drug	Madecassol	COL2A1 COL1A1 COL1A2	2.18e-05	46	27	3	CID000108062
Drug	d-indobufen	COL2A1 COL1A1 COL1A2	2.81e-05	50	27	3	CID000044562
Drug	Oi-1	COL1A1 COL1A2	2.83e-05	7	27	2	CID000448053
Drug	ridogrel	COL2A1 COL1A1 COL1A2	3.16e-05	52	27	3	CID005362391
Drug	NSC49633	COL2A1 COL1A1 COL1A2	3.35e-05	53	27	3	CID000023340
Drug	desmosine	COL2A1 COL1A1 COL1A2	3.35e-05	53	27	3	CID000025435
Drug	3,4,5-trihydroxy-N-(4-(thiazol-2-ylsulfamoyl)-phenyl)-benzamide	COL2A1 COL1A1	3.78e-05	8	27	2	ctd:C000594958
Drug	dihydrocytochalasin B	COL2A1 RCC2 COL1A2	4.39e-05	58	27	3	CID000003064
Drug	4-hydroxymercuribenzoate	COL1A1 COL1A2	4.85e-05	9	27	2	ctd:C030601
Drug	AC1LAKND	COL2A1 COL1A1 COL1A2	5.37e-05	62	27	3	CID000470146
Drug	4-aminoazobenzene	COL2A1 COL1A1 COL1A2	6.47e-05	66	27	3	CID000006051
Drug	BAPN	COL2A1 COL1A1 COL1A2	8.06e-05	71	27	3	CID000001647
Drug	malotilate	COL2A1 COL1A1 COL1A2	8.06e-05	71	27	3	CID000004006
Drug	Pempidine tartrate [546-48-5]; Up 200; 13uM; MCF7; HT_HG-U133A	COL2A1 NSUN7 COL1A1 COL1A2	8.16e-05	197	27	4	3832_UP
Drug	Sulindac [38194-50-2]; Up 200; 11.2uM; MCF7; HT_HG-U133A	ELOA2 KIF13A ADAMTSL4 COL1A1	8.16e-05	197	27	4	5528_UP
Drug	estradiol, USP; Up 200; 0.01uM; HL60; HT_HG-U133A	TRIOBP CR1 COL1A1 COL1A2	8.32e-05	198	27	4	6200_UP
Drug	Etanidazole [22668-01-5]; Up 200; 18.6uM; PC3; HT_HG-U133A	COL2A1 RIPOR2 ADAMTSL4 COL1A1	8.65e-05	200	27	4	5730_UP
Drug	L-3,4-dehydroproline	COL2A1 COL1A1 COL1A2	8.75e-05	73	27	3	CID000094284
Drug	AC1NMZ1B	COL2A1 COL1A1 COL1A2	9.49e-05	75	27	3	CID005034185
Drug	strontium ranelate	COL2A1 COL1A1 COL1A2	1.03e-04	77	27	3	CID006918182
Drug	halofuginone lactate	COL2A1 COL1A1 COL1A2	1.38e-04	85	27	3	CID000062891
Drug	4-hydroxyproline	COL2A1 COL1A1 COL1A2	1.69e-04	91	27	3	CID000000825
Drug	Rgd Peptide	COL2A1 ADAMTSL4 COL1A1 COL1A2	1.72e-04	239	27	4	CID000104802
Drug	alizarin red S	COL2A1 COL1A1 COL1A2	1.91e-04	95	27	3	CID000008534
Drug	Taylor's blue	COL2A1 COL1A1	2.05e-04	18	27	2	CID000123898
Drug	deoxypyridinoline	COL2A1 COL1A1 COL1A2	2.10e-04	98	27	3	CID000105071
Drug	pyridinoline	COL2A1 COL1A1 COL1A2	2.16e-04	99	27	3	CID000105068
Drug	didecyldimethylammonium	COL1A1 COL1A2	2.29e-04	19	27	2	ctd:C027118
Drug	AC1L9N61	COL2A1 COL1A1 COL1A2	2.36e-04	102	27	3	CID000449471
Drug	ticlopidine	COL2A1 COL1A1 COL1A2	2.43e-04	103	27	3	CID000005472
Drug	351A	COL2A1 COL1A1	2.54e-04	20	27	2	CID000122144
Drug	S-Adenosylhomocysteine	COL1A1 COL1A2	2.54e-04	20	27	2	ctd:D012435
Drug	hydroxylysine	COL2A1 COL1A1 COL1A2	2.87e-04	109	27	3	CID000001029
Drug	bromochloroacetic acid	COL2A1 COL1A1 COL1A2	2.87e-04	109	27	3	ctd:C099813
Drug	AC1L1C2F	COL2A1 COL1A1 COL1A2	2.95e-04	110	27	3	CID000001711
Drug	Sudan II	COL2A1 NALF2 COL1A1	3.19e-04	113	27	3	CID005354447
Drug	PPACK	COL2A1 COL1A1 COL1A2	3.19e-04	113	27	3	CID003036757
Drug	AC1L9732	COL2A1 COL1A1 COL1A2	3.28e-04	114	27	3	CID000439300
Drug	Tranilast sodium	COL2A1 COL1A1 COL1A2	3.36e-04	115	27	3	CID000005527
Drug	ABT-100	COL2A1 COL1A1	3.68e-04	24	27	2	CID006451154
Drug	exoenzyme C3, Clostridium botulinum	COL1A1 COL1A2	4.00e-04	25	27	2	ctd:C063007
Drug	farnesol pyrophosphate	COL2A1 SAMHD1 COL1A1	4.19e-04	124	27	3	CID000000706
Drug	Selara	COL2A1 COL1A1 COL1A2	4.29e-04	125	27	3	CID000150310
Drug	fulvic acid	COL2A1 COL1A1	4.67e-04	27	27	2	ctd:C005023
Drug	[(2R,3R,4R,5S,6R)-2-[[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2-tritioacetyl)amino]oxan-4-yl] (3R)-3-hydroxydecanoate	COL1A1 COL1A2	5.02e-04	28	27	2	CID011650719
Drug	DMSe	COL2A1 COL1A1 COL1A2	5.03e-04	132	27	3	CID000020796
Disease	osteogenesis imperfecta type 3 (is_implicated_in)	COL1A1 COL1A2	8.06e-07	2	27	2	DOID:0110339 (is_implicated_in)
Disease	osteogenesis imperfecta type 4 (is_implicated_in)	COL1A1 COL1A2	8.06e-07	2	27	2	DOID:0110340 (is_implicated_in)
Disease	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE	COL1A1 COL1A2	8.06e-07	2	27	2	C0268345
Disease	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1	COL1A1 COL1A2	8.06e-07	2	27	2	C4551623
Disease	osteogenesis imperfecta type 2 (is_implicated_in)	COL1A1 COL1A2	8.06e-07	2	27	2	DOID:0110341 (is_implicated_in)
Disease	OSTEOGENESIS IMPERFECTA, TYPE IV	COL1A1 COL1A2	8.06e-07	2	27	2	166220
Disease	Osteogenesis imperfecta with normal sclerae, dominant form	COL1A1 COL1A2	8.06e-07	2	27	2	cv:C0268363
Disease	Osteogenesis imperfecta type III	COL1A1 COL1A2	8.06e-07	2	27	2	cv:C0268362
Disease	OSTEOGENESIS IMPERFECTA, TYPE II	COL1A1 COL1A2	8.06e-07	2	27	2	166210
Disease	Osteogenesis imperfecta, perinatal lethal	COL1A1 COL1A2	8.06e-07	2	27	2	cv:C0268358
Disease	OSTEOGENESIS IMPERFECTA, TYPE III	COL1A1 COL1A2	8.06e-07	2	27	2	259420
Disease	osteogenesis imperfecta (is_implicated_in)	COL1A1 COL1A2	2.42e-06	3	27	2	DOID:12347 (is_implicated_in)
Disease	osteogenesis imperfecta type 3 (implicated_via_orthology)	COL1A1 COL1A2	2.42e-06	3	27	2	DOID:0110339 (implicated_via_orthology)
Disease	OSTEOPOROSIS	COL1A1 COL1A2	4.83e-06	4	27	2	166710
Disease	Osteogenesis imperfecta, dominant perinatal lethal	COL1A1 COL1A2	8.05e-06	5	27	2	C0268358
Disease	Lobstein Disease	COL1A1 COL1A2	8.05e-06	5	27	2	C0023931
Disease	osteogenesis imperfecta (implicated_via_orthology)	COL1A1 COL1A2	8.05e-06	5	27	2	DOID:12347 (implicated_via_orthology)
Disease	Ehlers-Danlos Syndrome	COL1A1 COL1A2	8.05e-06	5	27	2	C0013720
Disease	Ehlers-Danlos syndrome (implicated_via_orthology)	COL1A1 COL1A2	1.21e-05	6	27	2	DOID:13359 (implicated_via_orthology)
Disease	Osteoporosis	COL1A1 COL1A2	1.21e-05	6	27	2	cv:C0029456
Disease	Osteogenesis imperfecta type IV (disorder)	COL1A1 COL1A2	3.61e-05	10	27	2	C0268363
Disease	Osteogenesis imperfecta type III (disorder)	COL1A1 COL1A2	4.41e-05	11	27	2	C0268362
Disease	basophil percentage of granulocytes	ZNF469 ZDHHC18 CHD7	5.98e-05	83	27	3	EFO_0007995
Disease	Osteogenesis Imperfecta	COL1A1 COL1A2	6.25e-05	13	27	2	C0029434
Disease	basophil percentage of leukocytes	ZNF469 ZDHHC18 CHD7 GLCCI1	6.78e-05	243	27	4	EFO_0007992
Disease	Oral Submucous Fibrosis	COL1A1 COL1A2	1.22e-04	18	27	2	C0029172
Disease	Osteogenesis imperfecta	COL1A1 COL1A2	1.68e-04	21	27	2	cv:C0029434
Disease	tooth agenesis	THSD7B NALF2	1.84e-04	22	27	2	EFO_0005410
Disease	Sensorineural Hearing Loss (disorder)	COL2A1 RIPOR2	2.02e-04	23	27	2	C0018784
Disease	neutrophil percentage of leukocytes	COL2A1 ZDHHC18 CHD7 RIPOR2 GLCCI1	2.06e-04	610	27	5	EFO_0007990
Disease	Heart valve disease	COL1A1 COL1A2	2.59e-04	26	27	2	C0018824
Disease	lymphocyte percentage of leukocytes	ZDHHC18 SAMHD1 CHD7 RIPOR2 GLCCI1	3.06e-04	665	27	5	EFO_0007993
Disease	Hereditary hearing loss and deafness	COL2A1 TRIOBP RIPOR2	3.18e-04	146	27	3	cv:C0236038
Disease	osteoporosis (is_implicated_in)	COL1A1 COL1A2	3.69e-04	31	27	2	DOID:11476 (is_implicated_in)
Disease	cortical thickness	TRIOBP ZNF469 CHD7 RIPOR2 KIF13A KIAA1614	4.26e-04	1113	27	6	EFO_0004840
Disease	macula measurement	COL2A1 GLCCI1 INVS	6.75e-04	189	27	3	EFO_0008375
Disease	ureteral obstruction (biomarker_via_orthology)	COL1A1 COL1A2	7.79e-04	45	27	2	DOID:5199 (biomarker_via_orthology)

Protein segments in the cluster

Peptide	Gene	Start	Entry
RKRPCNSQPCSQRPD	ADAMTSL4	1016	Q6UY14
PERRSPGSPVCRADK	GLCCI1	141	Q86VQ1
CEASNPRPEKGDRRP	CEP170B	141	Q9Y4F5
SDSEEKPCAKPRRPQ	CHD7	1581	Q9P2D1
SPEGSRKNPARTCRD	COL2A1	1271	P02458
PAGRKRERPERCSSS	RCC2	31	Q9P258
KFRRQSEDPSCPNER	ANO6	251	Q4KMQ2
PRAERKCPRIAPADS	ELOA2	151	Q8IYF1
RSPARDPRTTPACRD	KIAA1614	406	Q5VZ46
APRPSDKPCADSERA	NALF2	26	O75949
TPEGSRKNPARTCRD	COL1A2	1151	P08123
EESPQPRRKRQPSSS	CUSTOS	136	Q96C57
KDRCRRKSCRNPPDP	CR1	96	P17927
DESCPAPQRQRPCRK	ANKS3	246	Q6ZW76
AEQQKGRRSPDSCRP	INVS	606	Q9Y283
LPRDSPRRNKEGCTS	KIF13A	1431	Q9H1H9
SEKPAQSLDPSRRPR	PPP1R12C	581	Q9BZL4
SEQPSKRPRCDDSPR	SAMHD1	6	Q9Y3Z3
KRPRCDDSPRTPSNT	SAMHD1	11	Q9Y3Z3
PAFVKNTCPSRPRER	NSUN7	616	Q8NE18
DSPRTSCARRDDPRA	TRIOBP	646	Q9H2D6
EEPRKPASAPSEACR	RIPOR2	506	Q9Y4F9
RSPEGSRKNPARTCR	COL1A1	1246	P02452
RKCAARDPEDRIPSP	RRP7A	6	Q9Y3A4
NRSREACKDRTPPPR	RPS26P11	86	Q5JNZ5
VGRSRPKANSRPDCD	TTLL3	671	Q9Y4R7
ERAKPRARSTPSNPD	ZNF469	3241	Q96JG9
KRCPDSTRPETVRPC	THSD7B	716	Q9C0I4
SPIRSDEPACRAKPD	ZDHHC18	366	Q9NUE0