Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
GeneOntologyMolecularFunction	transcription coactivator activity	ARID1B FIZ1 SMARCD2 WBP2NL ZMIZ1 MAML3	9.39e-05	303	49	6	GO:0003713
GeneOntologyMolecularFunction	molecular adaptor activity	BHLHE41 ARID1B PDCD6 SNAP91 FIZ1 SMARCD2 WBP2NL ZMIZ1 AHDC1 MAML3 COL1A2	3.60e-04	1356	49	11	GO:0060090
GeneOntologyMolecularFunction	platelet-derived growth factor binding	COL1A1 COL1A2	3.83e-04	12	49	2	GO:0048407
GeneOntologyMolecularFunction	transcription coregulator activity	BHLHE41 ARID1B FIZ1 SMARCD2 WBP2NL ZMIZ1 MAML3	4.15e-04	562	49	7	GO:0003712
GeneOntologyMolecularFunction	protein-macromolecule adaptor activity	BHLHE41 ARID1B PDCD6 SNAP91 FIZ1 SMARCD2 WBP2NL ZMIZ1 MAML3 COL1A2	4.34e-04	1160	49	10	GO:0030674
GeneOntologyMolecularFunction	DNA-binding transcription factor activity, RNA polymerase II-specific	FOXD2 BHLHE41 SCRT1 FOXO6 HELT NKX1-1 TPRX2 DMRTA2 NR2F1 FOXD1 FOSL1	5.08e-04	1412	49	11	GO:0000981
GeneOntologyMolecularFunction	RNA polymerase II cis-regulatory region sequence-specific DNA binding	FOXD2 BHLHE41 SCRT1 FOXO6 HELT NKX1-1 DMRTA2 NR2F1 FOXD1 FOSL1	7.49e-04	1244	49	10	GO:0000978
GeneOntologyMolecularFunction	cis-regulatory region sequence-specific DNA binding	FOXD2 BHLHE41 SCRT1 FOXO6 HELT NKX1-1 DMRTA2 NR2F1 FOXD1 FOSL1	8.85e-04	1271	49	10	GO:0000987
GeneOntologyMolecularFunction	structural constituent of nuclear pore	NUP214 POM121C	1.71e-03	25	49	2	GO:0017056
GeneOntologyMolecularFunction	nuclear localization sequence binding	NUP214 POM121C	1.99e-03	27	49	2	GO:0008139
GeneOntologyMolecularFunction	RNA polymerase II transcription regulatory region sequence-specific DNA binding	FOXD2 BHLHE41 SCRT1 FOXO6 HELT NKX1-1 DMRTA2 NR2F1 FOXD1 FOSL1	2.50e-03	1459	49	10	GO:0000977
GeneOntologyBiologicalProcess	skin morphogenesis	AHDC1 COL1A1 COL1A2	5.62e-06	15	49	3	GO:0043589
GeneOntologyBiologicalProcess	vitellogenesis	ZMIZ1 FOSL1	3.31e-05	4	49	2	GO:0007296
GeneOntologyBiologicalProcess	regionalization	BHLHE41 ANKS6 HELT DMRTA2 NR2F1 LFNG FOXD1	1.27e-04	478	49	7	GO:0003002
GeneOntologyBiologicalProcess	cerebral cortex regionalization	DMRTA2 NR2F1	1.97e-04	9	49	2	GO:0021796
GeneOntologyBiologicalProcess	pattern specification process	BHLHE41 ANKS6 HELT DMRTA2 NR2F1 LFNG FOXD1	2.29e-04	526	49	7	GO:0007389
GeneOntologyCellularComponent	chromatin	FOXD2 BHLHE41 ARID1B FOXO6 CPSF6 HELT FIZ1 NKX1-1 SMARCD2 DMRTA2 TAF4 ZMIZ1 FOXD1 FOSL1	4.79e-06	1480	49	14	GO:0000785
GeneOntologyCellularComponent	collagen type I trimer	COL1A1 COL1A2	5.38e-06	2	49	2	GO:0005584
GeneOntologyCellularComponent	bBAF complex	ARID1B SMARCD2	2.39e-04	10	49	2	GO:0140092
GeneOntologyCellularComponent	fibrillar collagen trimer	COL1A1 COL1A2	3.50e-04	12	49	2	GO:0005583
GeneOntologyCellularComponent	banded collagen fibril	COL1A1 COL1A2	3.50e-04	12	49	2	GO:0098643
GeneOntologyCellularComponent	brahma complex	ARID1B SMARCD2	4.81e-04	14	49	2	GO:0035060
GeneOntologyCellularComponent	vesicle coat	PDCD6 COPA SNAP91	5.22e-04	67	49	3	GO:0030120
GeneOntologyCellularComponent	complex of collagen trimers	COL1A1 COL1A2	1.10e-03	21	49	2	GO:0098644
GeneOntologyCellularComponent	coated vesicle	CPNE2 PDCD6 COPA SNAP91 SNX18	1.51e-03	360	49	5	GO:0030135
GeneOntologyCellularComponent	membrane coat	PDCD6 COPA SNAP91	1.97e-03	106	49	3	GO:0030117
GeneOntologyCellularComponent	coated membrane	PDCD6 COPA SNAP91	1.97e-03	106	49	3	GO:0048475
GeneOntologyCellularComponent	SWI/SNF complex	ARID1B SMARCD2	2.25e-03	30	49	2	GO:0016514
HumanPheno	Biconcave flattened vertebrae	COL1A1 COL1A2	1.05e-05	2	17	2	HP:0003321
HumanPheno	Severe generalized osteoporosis	COL1A1 COL1A2	1.05e-05	2	17	2	HP:0005897
HumanPheno	Absent ossification of calvaria	COL1A1 COL1A2	1.05e-05	2	17	2	HP:0005623
HumanPheno	Femoral bowing present at birth, straightening with time	COL1A1 COL1A2	1.05e-05	2	17	2	HP:0005005
HumanPheno	Popcorn calcification	COL1A1 COL1A2	3.14e-05	3	17	2	HP:6000871
HumanPheno	Bowing of limbs due to multiple fractures	COL1A1 COL1A2	6.27e-05	4	17	2	HP:0003023
HumanPheno	Cortical thickening of long bone diaphyses	MAN2B1 COL1A1	1.04e-04	5	17	2	HP:0005791
HumanPheno	Basilar impression	COL1A1 COL1A2	1.04e-04	5	17	2	HP:0005758
HumanPheno	Contracture of the proximal interphalangeal joint of the 2nd finger	LFNG COL1A1	1.04e-04	5	17	2	HP:0009540
HumanPheno	Flexion contracture of the 2nd finger	LFNG COL1A1	1.04e-04	5	17	2	HP:0009537
HumanPheno	Prominent interphalangeal joints	ARID1B TAF4	1.56e-04	6	17	2	HP:0006237
HumanPheno	Crumpled long bones	COL1A1 COL1A2	1.56e-04	6	17	2	HP:0006367
HumanPheno	Coxa valga	ARID1B MAN2B1 COL1A1 COL1A2	1.98e-04	92	17	4	HP:0002673
HumanPheno	Otosclerosis	COL1A1 COL1A2	2.18e-04	7	17	2	HP:0000362
HumanPheno	Arterial rupture	COL1A1 COL1A2	2.90e-04	8	17	2	HP:0025019
HumanPheno	Inguinal hernia	ARID1B MAN2B1 TAF4 LFNG COL1A1 COL1A2	3.50e-04	312	17	6	HP:0000023
HumanPheno	Soft skin	MAN2B1 COL1A1 COL1A2	3.76e-04	44	17	3	HP:0000977
HumanPheno	Deviation of toes	TAF4 ZMIZ1 COL1A1 COL1A2	5.16e-04	118	17	4	HP:0100498
HumanPheno	Femoral bowing	MAN2B1 COL1A1 COL1A2	5.49e-04	50	17	3	HP:0002980
HumanPheno	Multiple rib fractures	COL1A1 COL1A2	5.67e-04	11	17	2	HP:0006640
HumanPheno	Platyspondyly	MAN2B1 LFNG COL1A1 COL1A2	6.23e-04	124	17	4	HP:0000926
HumanPheno	Expressive language delay	ARID1B TAF4 AHDC1	7.67e-04	56	17	3	HP:0002474
HumanPheno	Language delay	ARID1B TAF4 AHDC1	7.67e-04	56	17	3	HP:0002336
HumanPheno	Thickened cortex of long bones	MAN2B1 COL1A1	8.00e-04	13	17	2	HP:0000935
HumanPheno	Protrusio acetabuli	COL1A1 COL1A2	8.00e-04	13	17	2	HP:0003179
HumanPheno	Thickened cortex of bones	MAN2B1 COL1A1	8.00e-04	13	17	2	HP:0100039
HumanPheno	Recurrent joint dislocation	COL1A1 COL1A2	9.32e-04	14	17	2	HP:0031869
HumanPheno	Neonatal short-limb short stature	COL1A1 COL1A2	9.32e-04	14	17	2	HP:0008921
HumanPheno	Soft, doughy skin	COL1A1 COL1A2	9.32e-04	14	17	2	HP:0001027
HumanPheno	Retrognathia	ARID1B SPEG TAF4 NR2F1 COL1A1 COL1A2	9.41e-04	375	17	6	HP:0000278
MousePheno	slow extinction of fear memory	ARID1B NR2F1	2.51e-05	3	41	2	MP:0012318
MousePheno	abnormal compact bone lamellar structure	COL1A1 COL1A2	8.35e-05	5	41	2	MP:0010970
MousePheno	decreased tendon stiffness	COL1A1 COL1A2	8.35e-05	5	41	2	MP:0003098
MousePheno	abnormal tendon physiology	COL1A1 COL1A2	1.25e-04	6	41	2	MP:0030802
MousePheno	abnormal tendon stiffness	COL1A1 COL1A2	1.25e-04	6	41	2	MP:0003097
Domain	TF_fork_head_CS_1	FOXD2 FOXO6 FOXD1	2.24e-04	47	47	3	IPR018122
Domain	FH	FOXD2 FOXO6 FOXD1	2.54e-04	49	47	3	SM00339
Domain	FORK_HEAD_1	FOXD2 FOXO6 FOXD1	2.54e-04	49	47	3	PS00657
Domain	FORK_HEAD_2	FOXD2 FOXO6 FOXD1	2.54e-04	49	47	3	PS00658
Domain	Fork_head_dom	FOXD2 FOXO6 FOXD1	2.54e-04	49	47	3	IPR001766
Domain	FORK_HEAD_3	FOXD2 FOXO6 FOXD1	2.54e-04	49	47	3	PS50039
Domain	Forkhead	FOXD2 FOXO6 FOXD1	2.54e-04	49	47	3	PF00250
Domain	Fib_collagen_C	COL1A1 COL1A2	3.36e-04	11	47	2	IPR000885
Domain	COLFI	COL1A1 COL1A2	3.36e-04	11	47	2	PF01410
Domain	NC1_FIB	COL1A1 COL1A2	3.36e-04	11	47	2	PS51461
Domain	Fib_collagen_C	COL1A1 COL1A2	3.36e-04	11	47	2	PD002078
Domain	COLFI	COL1A1 COL1A2	3.36e-04	11	47	2	SM00038
Domain	Hairy_orange	BHLHE41 HELT	4.03e-04	12	47	2	PF07527
Domain	Orange_dom	BHLHE41 HELT	4.03e-04	12	47	2	IPR003650
Domain	ORANGE	BHLHE41 HELT	4.75e-04	13	47	2	PS51054
Pathway	REACTOME_ENHANCED_BINDING_OF_GP1BA_VARIANT_TO_VWF_MULTIMER_COLLAGEN	COL1A1 COL1A2	1.40e-04	7	37	2	M48265
Pathway	REACTOME_DEFECTS_OF_PLATELET_ADHESION_TO_EXPOSED_COLLAGEN	COL1A1 COL1A2	1.86e-04	8	37	2	M48236
Pathway	REACTOME_GP1B_IX_V_ACTIVATION_SIGNALLING	COL1A1 COL1A2	4.35e-04	12	37	2	MM15093
Pathway	REACTOME_GP1B_IX_V_ACTIVATION_SIGNALLING	COL1A1 COL1A2	4.35e-04	12	37	2	M27352
Pathway	REACTOME_PLATELET_ADHESION_TO_EXPOSED_COLLAGEN	COL1A1 COL1A2	4.35e-04	12	37	2	MM15452
Pathway	REACTOME_ANCHORING_FIBRIL_FORMATION	COL1A1 COL1A2	6.89e-04	15	37	2	M27161
Pathway	REACTOME_PLATELET_ADHESION_TO_EXPOSED_COLLAGEN	COL1A1 COL1A2	7.86e-04	16	37	2	M9450
Pathway	REACTOME_CROSSLINKING_OF_COLLAGEN_FIBRILS	COL1A1 COL1A2	9.99e-04	18	37	2	M27164
Pathway	REACTOME_CROSSLINKING_OF_COLLAGEN_FIBRILS	COL1A1 COL1A2	9.99e-04	18	37	2	MM14882
Pathway	REACTOME_DISEASES_OF_HEMOSTASIS	COL1A1 COL1A2	1.11e-03	19	37	2	M48230
Pathway	REACTOME_SCAVENGING_BY_CLASS_A_RECEPTORS	COL1A1 COL1A2	1.11e-03	19	37	2	M27221
Pathway	REACTOME_MET_ACTIVATES_PTK2_SIGNALING	COL1A1 COL1A2	1.11e-03	19	37	2	MM15512
Pubmed	Comparative Application of BioID and TurboID for Protein-Proximity Biotinylation.	PTGES2 ARID1B PDCD6 CPSF6 NUP214 ZMIZ1 POM121C AHDC1 MAML3	1.39e-08	457	49	9	32344865
Pubmed	Interaction network of human early embryonic transcription factors.	ARID1B SMARCD2 TPRX2 NUP214 TAF4 ZMIZ1 POM121C AHDC1	3.13e-08	351	49	8	38297188
Pubmed	FOXD1 promotes nephron progenitor differentiation by repressing decorin in the embryonic kidney.	FOXD1 COL1A1 COL1A2	3.13e-07	10	49	3	24284212
Pubmed	The Lin28/let-7 Pathway Regulates the Mammalian Caudal Body Axis Elongation Program.	TRIM71 FOXD1 COL1A1	5.73e-07	12	49	3	30661985
Pubmed	Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation.	FOSL1 COL1A1 COL1A2	1.18e-06	15	49	3	15866165
Pubmed	Complete primary structure of rainbow trout type I collagen consisting of alpha1(I)alpha2(I)alpha3(I) heterotrimers.	COL1A1 COL1A2	1.94e-06	2	49	2	11358497
Pubmed	Regulation of type I collagen genes expression.	COL1A1 COL1A2	1.94e-06	2	49	2	11143996
Pubmed	No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	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	1.94e-06	2	49	2	15211650
Pubmed	Identification of COL1A1 and COL1A2 as candidate prognostic factors in gastric cancer.	COL1A1 COL1A2	1.94e-06	2	49	2	27894325
Pubmed	[Expression and clinical significance of COL1A1 and COL1A2 genes in malignant pleural mesothelioma tissues].	COL1A1 COL1A2	1.94e-06	2	49	2	35915937
Pubmed	Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - genotype-phenotype correlations and effect of bisphosphonate treatment.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	2	10408781
Pubmed	Characterization of point mutations in the collagen COL1A1 and COL1A2 genes causing lethal perinatal osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	2777764
Pubmed	[Phenotype-genotype analysis and detection of gene variant in six families with osteogenesis imperfecta].	COL1A1 COL1A2	1.94e-06	2	49	2	32335875
Pubmed	Collagen gene polymorphisms influence fracture risk and bone mass acquisition during childhood and adolescent growth.	COL1A1 COL1A2	1.94e-06	2	49	2	20736093
Pubmed	[Analysis of COL1A1 and COL1A2 gene variants in two fetuses with osteogenesis imperfecta].	COL1A1 COL1A2	1.94e-06	2	49	2	37368383
Pubmed	Streptococcal protein FOG, a novel matrix adhesin interacting with collagen I in vivo.	COL1A1 COL1A2	1.94e-06	2	49	2	16278217
Pubmed	Osteogenesis imperfecta: comparison of molecular defects with bone histological changes.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	2	8723681
Pubmed	Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	36951356
Pubmed	Effects of GABA on the expression of type I collagen gene in normal human dermal fibroblasts.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	2	17211858
Pubmed	Msi2 Maintains Quiescent State of Hair Follicle Stem Cells by Directly Repressing the Hh Signaling Pathway.	MSI2 COL1A1	1.94e-06	2	49	2	28143780
Pubmed	Identification of COL1A1/2 Mutations and Fusions With Noncoding RNA Genes in Bizarre Parosteal Osteochondromatous Proliferation (Nora Lesion).	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	2	8094076
Pubmed	Inter- and Intrafamilial Phenotypic Variability in Individuals with Collagen-Related Osteogenesis Imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	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	1.94e-06	2	49	2	35909573
Pubmed	Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	27519266
Pubmed	Biochemical markers of bone turnover and clinical outcomes in men with prostate cancer.	COL1A1 COL1A2	1.94e-06	2	49	2	21163673
Pubmed	Mutation of the 5'-untranslated region stem-loop structure inhibits α1(I) collagen expression in vivo.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	2	9443882
Pubmed	COL1A1 and COL1A2 sequencing results in cohort of patients undergoing evaluation for potential child abuse.	COL1A1 COL1A2	1.94e-06	2	49	2	27090748
Pubmed	Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients.	COL1A1 COL1A2	1.94e-06	2	49	2	15241796
Pubmed	Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	24668929
Pubmed	Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	2	7945553
Pubmed	Relationship between genotype and skeletal phenotype in children and adolescents with osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	19929435
Pubmed	[Relationship of collagen type I alpha 1 and alpha 2 gene polymorphisms with bone mineral density].	COL1A1 COL1A2	1.94e-06	2	49	2	16864092
Pubmed	Cloning, characterization, and functional studies of a nonintegrin platelet receptor for type I collagen.	COL1A1 COL1A2	1.94e-06	2	49	2	9239397
Pubmed	Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxis.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	2	6857446
Pubmed	Genotype-phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I.	COL1A1 COL1A2	1.94e-06	2	49	2	20087402
Pubmed	Adhesion of human neuroblasts to HIV-1 tat.	COL1A1 COL1A2	1.94e-06	2	49	2	8552450
Pubmed	Responsiveness to pamidronate treatment is not related to the genotype of type I collagen in patients with osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	28528406
Pubmed	Clinical significance and biological role of cancer-derived Type I collagen in lung and esophageal cancers.	COL1A1 COL1A2	1.94e-06	2	49	2	30604926
Pubmed	Early type I collagen deposition is associated with prognosis in biliary atresia.	COL1A1 COL1A2	1.94e-06	2	49	2	26452701
Pubmed	Homology-mediated recombination between type I collagen gene exons results in an internal tandem duplication and lethal osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	8097422
Pubmed	[Analysis of gross deletions of COL1A1/2 genes in Chinese families affected with osteogenesis imperfecta].	COL1A1 COL1A2	1.94e-06	2	49	2	27454992
Pubmed	Regional chromosome mapping of human collagen genes alpha 2(I) and alpha 1(I) (COLIA2 and COLIA1).	COL1A1 COL1A2	1.94e-06	2	49	2	3857213
Pubmed	No evidence for disturbed COL1A1 and A2 expression in otosclerosis.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	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	1.94e-06	2	49	2	1874719
Pubmed	Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects.	COL1A1 COL1A2	1.94e-06	2	49	2	35044492
Pubmed	Differential unfolding of alpha1 and alpha2 chains in type I collagen and collagenolysis.	COL1A1 COL1A2	1.94e-06	2	49	2	18644377
Pubmed	COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	21344539
Pubmed	Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study.	COL1A1 COL1A2	1.94e-06	2	49	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	1.94e-06	2	49	2	23692737
Pubmed	Effects of antisense oligodeoxynucleotide to type I collagen gene on hypertrophic scars in the transplanted nude mouse model.	COL1A1 COL1A2	1.94e-06	2	49	2	19469869
Pubmed	Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers-Danlos syndrome.	COL1A1 COL1A2	1.94e-06	2	49	2	32091183
Pubmed	Deletions and duplications of Gly-Xaa-Yaa triplet repeats in the triple helical domains of type I collagen chains disrupt helix formation and result in several types of osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	11668615
Pubmed	Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.	COL1A1 COL1A2	1.94e-06	2	49	2	28498836
Pubmed	[Mutational analysis and prenatal diagnosis of COL1A1 and COL1A2 genes in four Chinese families affected with osteogenesis imperfecta].	COL1A1 COL1A2	1.94e-06	2	49	2	28981938
Pubmed	COL1-related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap.	COL1A1 COL1A2	1.94e-06	2	49	2	31794058
Pubmed	COL1A1 and COL1A2 variants in Ehlers-Danlos syndrome phenotypes and COL1-related overlap disorder.	COL1A1 COL1A2	1.94e-06	2	49	2	36896471
Pubmed	Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	16705691
Pubmed	Influence of type I collagen polymorphisms and risk of anterior cruciate ligament rupture in athletes: a case-control study.	COL1A1 COL1A2	1.94e-06	2	49	2	35172811
Pubmed	Chemical cleavage method for the detection of RNA base changes: experience in the application to collagen mutations in osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	8456808
Pubmed	Cranial base abnormalities in osteogenesis imperfecta: phenotypic and genotypic determinants.	COL1A1 COL1A2	1.94e-06	2	49	2	20721936
Pubmed	A cysteine-based molecular code informs collagen C-propeptide assembly.	COL1A1 COL1A2	1.94e-06	2	49	2	30310058
Pubmed	Four new cases of lethal osteogenesis imperfecta due to glycine substitutions in COL1A1 and genes. Mutations in brief no. 152. Online.	COL1A1 COL1A2	1.94e-06	2	49	2	10627137
Pubmed	Use of the Cre/lox recombination system to develop a non-lethal knock-in murine model for osteogenesis imperfecta with an alpha1(I) G349C substitution. Variability in phenotype in BrtlIV mice.	COL1A1 COL1A2	1.94e-06	2	49	2	10608859
Pubmed	Structural and mechanical differences between collagen homo- and heterotrimers: relevance for the molecular origin of brittle bone disease.	COL1A1 COL1A2	1.94e-06	2	49	2	22325288
Pubmed	Heterotrimeric type I collagen C-telopeptide conformation as docked to its helix receptor.	COL1A1 COL1A2	1.94e-06	2	49	2	15581348
Pubmed	Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	27748872
Pubmed	Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients.	COL1A1 COL1A2	1.94e-06	2	49	2	28810924
Pubmed	Mutation characteristics in type I collagen genes in Chinese patients with osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	21341209
Pubmed	The type I collagen pro alpha 1(I) COOH-terminal propeptide N-linked oligosaccharide. Functional analysis by site-directed mutagenesis.	COL1A1 COL1A2	1.94e-06	2	49	2	7629088
Pubmed	Structural basis of homo- and heterotrimerization of collagen I.	COL1A1 COL1A2	1.94e-06	2	49	2	28281531
Pubmed	Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	25944380
Pubmed	Deposition of apatite in mineralizing vertebrate extracellular matrices: A model of possible nucleation sites on type I collagen.	COL1A1 COL1A2	1.94e-06	2	49	2	21405976
Pubmed	The human type I collagen mutation database.	COL1A1 COL1A2	1.94e-06	2	49	2	9016532
Pubmed	The relationship between COLI A1 polymorphisms (Sp 1) and COLI A2 polymorphisms (Eco R1 and Puv II) with bone mineral density in Chinese men and women.	COL1A1 COL1A2	1.94e-06	2	49	2	15085313
Pubmed	Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene.	COL1A1 COL1A2	1.94e-06	2	49	2	8841196
Pubmed	Differential Protein Expression between Cystic and Solid Vestibular Schwannoma Using Tandem Mass Tag-Based Quantitative Proteomic Analysis.	COL1A1 COL1A2	1.94e-06	2	49	2	32157794
Pubmed	Osteogenesis imperfecta: translation of mutation to phenotype.	COL1A1 COL1A2	1.94e-06	2	49	2	1895312
Pubmed	Mutations in the COL1A1 and COL1A2 genes associated with osteogenesis imperfecta (OI) types I or III.	COL1A1 COL1A2	1.94e-06	2	49	2	29543922
Pubmed	Mutations in type I collagen genes in Japanese osteogenesis imperfecta patients.	COL1A1 COL1A2	1.94e-06	2	49	2	17875077
Pubmed	Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix.	COL1A1 COL1A2	1.94e-06	2	49	2	7881420
Pubmed	Positive association of collagen type I with non-muscle invasive bladder cancer progression.	COL1A1 COL1A2	1.94e-06	2	49	2	27655672
Pubmed	Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes.	COL1A1 COL1A2	1.94e-06	2	49	2	19714363
Pubmed	COL1A1/2 Osteogenesis Imperfecta	COL1A1 COL1A2	1.94e-06	2	49	2	20301472
Pubmed	Defective C-propeptides of the proalpha2(I) chain of type I procollagen impede molecular assembly and result in osteogenesis imperfecta.	COL1A1 COL1A2	1.94e-06	2	49	2	18375391
Pubmed	Genome-wide Identification of Foxf2 Target Genes in Palate Development.	FOXD1 COL1A1 COL1A2	4.56e-06	23	49	3	32040930
Pubmed	A mouse model of brittle cornea syndrome caused by mutation in Zfp469.	COL1A1 COL1A2	5.83e-06	3	49	2	34368841
Pubmed	Molecular mechanism of type I collagen homotrimer resistance to mammalian collagenases.	COL1A1 COL1A2	5.83e-06	3	49	2	20463013
Pubmed	Characterization of binding of LARP6 to the 5' stem-loop of collagen mRNAs: implications for synthesis of type I collagen.	COL1A1 COL1A2	5.83e-06	3	49	2	25692237
Pubmed	Inhibition of fibronectin binding and fibronectin-mediated cell adhesion to collagen by a peptide from the second type I repeat of thrombospondin.	COL1A1 COL1A2	5.83e-06	3	49	2	8468356
Interaction	NUP35 interactions	PTGES2 ARID1B CPSF6 NUP214 ZMIZ1 POM121C AHDC1 MAML3	6.49e-06	424	48	8	int:NUP35
Interaction	TGFBI interactions	KIF13B COL1A1 COL1A2	2.81e-05	25	48	3	int:TGFBI
GeneFamily	Forkhead boxes	FOXD2 FOXO6 FOXD1	9.20e-05	43	37	3	508
CoexpressionAtlas	DevelopingKidney_e15.5_Cap mesenchyme_emap-27738_top-relative-expression-ranked_1000	FOXD2 SNAP91 CPSF6 SPEG NUP214 ARHGAP39 TAF4 ZMIZ1 FOXD1 MSI2	6.30e-06	779	47	10	gudmap_developingKidney_e15.5_Cap mesenchyme_1000
ToppCell	droplet-Kidney-KIDNEY-1m-Epithelial-Pecam____kidney_capillary_endothelial_cell\|Kidney / Skin_Bladder_Kidney_Mammary_Gland - method, tissue, subtissue, age, lineage, cell ontology and free annotation	FOXD2 SPEG GPR88 NR2F1 FOXD1 COL1A2	4.59e-08	184	48	6	1c857126c0ea0671f0d60b048efca288d348d653
ToppCell	Mild/Remission-B_naive-8\|Mild/Remission / disease group and sub_cluster of B and Plasma cells(res = 0.5)	ARID1B FOXO6 SIPA1 AHDC1 MAML3 MSI2	6.47e-08	195	48	6	0a3221e4d1fa31a35868bdda0f0cc873c233b407
ToppCell	E16.5-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2-AF2_mature\|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	SCRT1 MAN2B1 GPR88 COL1A1 COL1A2	9.41e-07	165	48	5	4e13fccd32029e2879e85f8966e582a46c09e4aa
ToppCell	renal_cortex_nuclei-Adult_normal_reference-Mesenchymal-Myocytic_interstitial_cell-Degenerative_Vascular_Smooth_Muscle_Cell\|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group	FOXO6 RPLP1 SPEG PROB1 COL1A2	1.19e-06	173	48	5	3001dd39244ef0a5a475d569a78f4ae427a55db6
ToppCell	renal_cortex_nuclei-Adult_normal_reference-Mesenchymal-Myocytic_interstitial_cell-Degenerative_Vascular_Smooth_Muscle_Cell-\|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group	FOXO6 RPLP1 SPEG PROB1 COL1A2	1.19e-06	173	48	5	c88883fb2a33e21d4201aa393674aa3f2ad780c9
ToppCell	Tracheal-10x5prime-Stromal-Peri/Epineurial_-NAF_endoneurial\|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations	DIPK1C AHDC1 NR2F1 COL1A1 COL1A2	2.30e-06	198	48	5	7a0c4dbc8c99968d42af00a718f4fedc544599ec
ToppCell	distal-1-mesenchymal-Myofibroblast\|1 / Location, Lineage, Cell class (ontology) and Donor from 10X sequencing (macrophage renamed)	DIPK1C GPR88 NR2F1 COL1A1 COL1A2	2.36e-06	199	48	5	58c36f5a30c6862b7f5587a0b9bc31da99e43dd5
ToppCell	distal-mesenchymal-Myofibroblast-1\|distal / Location, Lineage, Cell class (ontology) and Donor from 10X sequencing (macrophage renamed)	DIPK1C GPR88 NR2F1 COL1A1 COL1A2	2.36e-06	199	48	5	79917b5225cb45b4a0ea937f79f1752346e4346e
ToppCell	primary_visual_cortex-Non-neuronal-leptomeningeal_cell-VLMC-VLMC_Osr1_Cd74\|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	FOXD2 FOXD1 COL1A1 COL1A2	7.23e-06	115	48	4	4c7d78a246f1b44846fb959359515ef185530053
ToppCell	Hippocampus-Endothelial-ENDOTHELIAL_TIP-Dcn_1-Dcn_1_1\|Hippocampus / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	1.32e-05	134	48	4	b959899c89d3a0363a3cd2309155280e0fe5ba88
ToppCell	Thalamus-Endothelial-ENDOTHELIAL_TIP-Dcn_1\|Thalamus / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	2.23e-05	153	48	4	e9c6fb5c41adb6595c66c3a917fe455348279e54
ToppCell	Thalamus-Endothelial-ENDOTHELIAL_TIP-Dcn_1-Dcn_1_1\|Thalamus / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	2.23e-05	153	48	4	b8b5ff7d2feea3e3a352fb5530e49f639fe1ff88
ToppCell	Thalamus-Endothelial-ENDOTHELIAL_TIP\|Thalamus / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	2.23e-05	153	48	4	2513edfae62a44e51d3556675a096723194c966c
ToppCell	Frontal_cortex-Endothelial-ENDOTHELIAL_TIP-Dcn_1\|Frontal_cortex / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	2.28e-05	154	48	4	65dbb60f636562eeba3dafadae9c0c7db2b27476
ToppCell	Hippocampus-Endothelial-ENDOTHELIAL_TIP-Dcn_1\|Hippocampus / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	2.59e-05	159	48	4	92049a8d8fc9997d8d0d76500c72596a9b2394e0
ToppCell	LPS_only-Stromal_mesenchymal-Matrix_Fibroblast-Proliferative_MatrixFB\|LPS_only / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2	RPLP1 NR2F1 COL1A1 COL1A2	2.79e-05	162	48	4	b24298910eb39ea5103ae24439b3901205ed55b6
ToppCell	renal_medulla_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Fibroblast-Degenerative_Fibroblast\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	NR2F1 LFNG COL1A1 COL1A2	2.92e-05	164	48	4	01a7c335897128d3478b8b9b44fb461cab493084
ToppCell	Globus_pallidus-Endothelial-ENDOTHELIAL_TIP-Dcn_1\|Globus_pallidus / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	2.99e-05	165	48	4	570483b43ccb5831feec9337b4664814431d40b1
ToppCell	Globus_pallidus-Endothelial-ENDOTHELIAL_TIP\|Globus_pallidus / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	2.99e-05	165	48	4	2026a9a07f4d314cc05c167e491312b373468e46
ToppCell	E16.5-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2\|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	SCRT1 MAN2B1 COL1A1 COL1A2	3.14e-05	167	48	4	fe3338f99f94c0dac37e3d649dfdce82e4a56022
ToppCell	Hippocampus-Endothelial-ENDOTHELIAL_TIP\|Hippocampus / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	3.21e-05	168	48	4	26aa96b2b547d11941cb803995ea3d302ee0518c
ToppCell	frontal_cortex-Non-neuronal-leptomeningeal_cell-VLMC-VLMC_Osr1_Mc5r\|frontal_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	FOXD2 FOXD1 COL1A1 COL1A2	3.21e-05	168	48	4	9930bd63b60c03f0152838a79eef77da1c2dd8e5
ToppCell	PND10-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2-AF2_mature\|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	FOXO6 GPR88 COL1A1 COL1A2	3.29e-05	169	48	4	031465190cd3623a25ef2b868daab8d932c8ff08
ToppCell	LPS-IL1RA+antiTNF-Stromal_mesenchymal-Matrix_Fibroblast-Proliferative_MatrixFB\|LPS-IL1RA+antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2	RPLP1 NR2F1 COL1A1 COL1A2	3.44e-05	171	48	4	59d79c3e36a4930af42ebc96f05570641b9fb864
ToppCell	PND10-Mesenchymal-Mesenchymal_structural-Fibroblastic-AF2\|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	FOXO6 GPR88 COL1A1 COL1A2	3.44e-05	171	48	4	15cb4670ff4234ac46aea8a5911138d6913c4482
ToppCell	-Donor_08\|World / lung cells shred on cell class, cell subclass, sample id	RPLP1 NR2F1 COL1A1 COL1A2	3.60e-05	173	48	4	88be9182fbb1bc83531cd41e59ea57c112a21d54
ToppCell	primary_visual_cortex-Non-neuronal-leptomeningeal_cell\|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	FOXD2 FOXD1 COL1A1 COL1A2	3.68e-05	174	48	4	2891ab2fd05eb4bbd239d1a2865f21ef7f2df39e
ToppCell	primary_visual_cortex-Non-neuronal-leptomeningeal_cell-VLMC\|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	FOXD2 FOXD1 COL1A1 COL1A2	3.68e-05	174	48	4	eade55f86ef1f7a5355ad65cec3aa6bfc5d3c62d
ToppCell	renal_cortex_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Fibroblast-Degenerative_Fibroblast-Degenerative_Fibroblast_26.46.91\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	RPLP1 LFNG FOXD1 COL1A1	3.76e-05	175	48	4	3031f1eef3cfef8a7e5f57e567cb0868d06cac38
ToppCell	renal_cortex_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Fibroblast-Degenerative_Fibroblast\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	NR2F1 FOXD1 COL1A1 COL1A2	3.85e-05	176	48	4	fcf324e6402819683f95e0dd94bf1f777c7f4c76
ToppCell	primary_visual_cortex-Non-neuronal-leptomeningeal_cell-VLMC-VLMC_Osr1_Mc5r\|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	FOXD2 FOXD1 COL1A1 COL1A2	3.94e-05	177	48	4	599cf7f5b774e197a1b43c98e4b9a8c1a618f38a
ToppCell	Posterior_cortex-Endothelial-ENDOTHELIAL_TIP\|Posterior_cortex / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	4.02e-05	178	48	4	cda7695411655bd6d0ba69e5041ca7530a9dad3a
ToppCell	facs-Brain_Non-Myeloid-Hippocampus-3m-Neuronal\|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation	CELF6 FOXO6 DMRTA2 MAML3	4.11e-05	179	48	4	69a1b3b05c921de6343ffe6ad998aa2b804312a7
ToppCell	BAL-Mild-cDC_4\|Mild / Compartment, Disease Groups and Clusters	ANKS6 NUP214 TAF4 SIPA1	4.11e-05	179	48	4	68511e87b12b8253de7771e5ccfc5869248b8450
ToppCell	facs-Brain_Non-Myeloid-Hippocampus-3m-Neuronal-neuron\|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation	CELF6 FOXO6 DMRTA2 MAML3	4.11e-05	179	48	4	479116ac65488c60104a053530830763ec1f95b2
ToppCell	facs-Brain_Non-Myeloid-Hippocampus-3m-Neuronal-nan\|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation	CELF6 FOXO6 DMRTA2 MAML3	4.11e-05	179	48	4	1dfc0cb8b369aef35c59f3d4c52603dc9f3728c1
ToppCell	renal_medulla_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Fibroblast-Degenerative_Fibroblast-Degenerative_Fibroblast_119\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	NR2F1 LFNG COL1A1 COL1A2	4.20e-05	180	48	4	ea7a1ccf0dd3bb5af5df87501f873e7339a824b3
ToppCell	P15-Mesenchymal-mesenchymal_fibroblast-mesenchymal_alveolar_niche_cell\|P15 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase	GPR88 FOXD1 COL1A1 COL1A2	4.39e-05	182	48	4	e9fcae9d03a6faf85b91882c5da699037bc61aeb
ToppCell	Pericytes-Cryobiopsy_01\|World / lung cells shred on cell class, cell subclass, sample id	SPEG NR2F1 COL1A1 COL1A2	4.39e-05	182	48	4	46c213597445b1f4f09dc367f27702d24b201daf
ToppCell	5'-Adult-LargeIntestine-Mesenchymal-fibroblastic-Stromal_3_(C7+)\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	GPR88 NR2F1 COL1A1 COL1A2	4.39e-05	182	48	4	3dfa9187e9d2bab1d199079d29209c4648220ada
ToppCell	droplet-Kidney-nan-21m-Epithelial-Pecam____kidney_capillary_endothelial_cell\|Kidney / Skin_Bladder_Kidney_Mammary_Gland - method, tissue, subtissue, age, lineage, cell ontology and free annotation	FOXD2 NR2F1 FOXD1 COL1A2	4.48e-05	183	48	4	f55081068213cc1cdb2acad58ff10f6b48b44c72
ToppCell	facs-Liver-Non-hepatocytes-24m-Endothelial-nan\|Liver / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation	GPR88 FOSL1 COL1A1 COL1A2	4.48e-05	183	48	4	ebe369dc80c4fbf8f4dbe947147f8c47507ffb60
ToppCell	Frontal_cortex-Endothelial-ENDOTHELIAL_TIP\|Frontal_cortex / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1 COL1A2	4.58e-05	184	48	4	235890e8b424f4386b6ea52d173d20a00898df73
ToppCell	droplet-Lung-21m-Mesenchymal-fibroblast-adventitial_fibroblast-adventitial_fibroblast_l17\|21m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype	ANKS6 GPR88 COL1A1 COL1A2	4.67e-05	185	48	4	1b990e3089772be2b38c6d7ea0d1bf22461ae3ea
ToppCell	P03-Mesenchymal-mesenchymal_fibroblast-mesenchymal_alveolar_niche_cell\|P03 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase	RPLP1 FOXD1 COL1A1 COL1A2	4.77e-05	186	48	4	c0a036096c2cb23305605b8aaf18869d6e0fb512
ToppCell	pdx\|World / Sample and Cell Type and Tumor Cluster (all cells)	ARID1B ASPSCR1 MAML3 MSI2	4.77e-05	186	48	4	de8e538c8767d41b8a52f5e58ba1affd4e7244c4
ToppCell	pdx-Tumor_cells\|World / Sample and Cell Type and Tumor Cluster (all cells)	ARID1B ASPSCR1 MAML3 MSI2	4.77e-05	186	48	4	0b88a87158a9ca8de3bf40a4ff1687150707a5f0
ToppCell	Control-Fibroblasts-Pathological_FB\|Control / group, cell type (main and fine annotations)	RPLP1 NR2F1 COL1A1 COL1A2	4.87e-05	187	48	4	b7280b8baa0fba9c2b4bff660c240ed96f6ff9b7
ToppCell	COVID-19_Mild-Neu_4\|COVID-19_Mild / 5 Neutrophil clusters in COVID-19 patients	CPNE2 RPLP1 WBP2NL LFNG	4.87e-05	187	48	4	714851e757c71c559ee6413a3f61d6c117c79ad2
ToppCell	renal_cortex_nuclei-Renal_AKI_(acute_kidney_injury)-Mesenchymal-Fibroblast-Degenerative_Fibroblast\|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group	RPLP1 NR2F1 COL1A1 COL1A2	5.08e-05	189	48	4	9e1a51997ef9b6999d9b40cf0a55e561e3b4a84c
ToppCell	renal_cortex_nuclei-Renal_AKI_(acute_kidney_injury)-Mesenchymal-Myocytic_interstitial_cell\|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group	SPEG NR2F1 COL1A1 COL1A2	5.18e-05	190	48	4	70c86dd454afb21d4a85db56c5f369d4b342bc97
ToppCell	renal_cortex_nuclei-Renal_AKI_(acute_kidney_injury)-Mesenchymal-Fibroblast-Degenerative_Fibroblast-Degenerative_Fibroblast_119\|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group	RPLP1 NR2F1 COL1A1 COL1A2	5.18e-05	190	48	4	7f6dafd5418764d67f6d5ec2153233b791910e81
ToppCell	Pericytes\|World / lung cells shred on cell class, cell subclass, sample id	SPEG NR2F1 COL1A1 COL1A2	5.40e-05	192	48	4	057ad22b878c0c5fb59ed1412ca13db945c57a5a
ToppCell	Tracheal-NucSeq-Stromal-Peri/Epineurial_-NAF_endoneurial\|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations	FOXD2 SIPA1 NR2F1 COL1A2	5.51e-05	193	48	4	549a0b750c860b615aff767ad04c9a9d20f802f0
ToppCell	facs-Lung-3m\|Lung / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype	ARID1B PAN3 COL1A1 COL1A2	5.73e-05	195	48	4	c4648c0332c3826776f9ad3f5f803dbac2b4c0c0
ToppCell	renal_medulla_nuclei-Renal_AKI_(acute_kidney_injury)-Mesenchymal-Fibroblast-high_collagen-matrisome_fibroblast-\|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group	NR2F1 LFNG COL1A1 COL1A2	5.85e-05	196	48	4	a12dd986df65c36f248cf10815c3b8b6238613b0
ToppCell	15-Distal-Mesenchymal-Airway_Smooth_Muscle\|Distal / Age, Tissue, Lineage and Cell class	RPLP1 SPEG MSI2 COL1A2	5.85e-05	196	48	4	0e45817625b96d21a8cc4dfbbd465ee6403b6802
ToppCell	renal_medulla_nuclei-Renal_AKI_(acute_kidney_injury)-Mesenchymal-Fibroblast-high_collagen-matrisome_fibroblast\|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group	NR2F1 LFNG COL1A1 COL1A2	5.85e-05	196	48	4	3e6803587d8566fd08cb8b290be3b6461743d79c
ToppCell	15-Distal-Mesenchymal\|Distal / Age, Tissue, Lineage and Cell class	RPLP1 NR2F1 COL1A1 COL1A2	5.85e-05	196	48	4	b8d95b5f4780e73d16dcc528e70a5496f0314373
ToppCell	Tracheal-10x5prime-Stromal-Peri/Epineurial_\|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations	DIPK1C AHDC1 NR2F1 COL1A2	5.97e-05	197	48	4	2cb1f557ce1400398975de94638126b4522567f3
ToppCell	renal_cortex_nuclei-CKD+DKD_normotensive-Mesenchymal-Fibroblast-Collagen+matrisome-high_fibroblast-\|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group	NR2F1 FOXD1 COL1A1 COL1A2	5.97e-05	197	48	4	85a8f1d18e0dd1d31341f5131eecd217553bf042
ToppCell	facs-Brain_Myeloid-Cortex_-18m-Myeloid-microglial_cell\|Brain_Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation	MAN2B1 SNX18 SIPA1 LFNG	5.97e-05	197	48	4	173c0c8de4e69882a9f91189deeb4a651fefe551
ToppCell	10x3'2.3-week_14-16-Mesenchymal_osteo-stroma-osteochondral_precursor\|week_14-16 / cell types per 3 fetal stages;per 3',per 5'	DIPK1C FOXD1 COL1A1 COL1A2	5.97e-05	197	48	4	c165c6fd12dc649b39e920d8528e2eb65c61956b
ToppCell	renal_cortex_nuclei-CKD+DKD_normotensive-Mesenchymal-Fibroblast-Collagen+matrisome-high_fibroblast\|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group	NR2F1 FOXD1 COL1A1 COL1A2	5.97e-05	197	48	4	e8e3ba791dfaa0fab35e0329a5e34376f9ee6143
ToppCell	IPF-Stromal-Myofibroblast\|Stromal / Disease state, Lineage and Cell class	KIF13B NR2F1 COL1A1 COL1A2	5.97e-05	197	48	4	f304d42fc4936fe20996e07c8dccc698a6e5e5ef
ToppCell	LPS_IL1RA_TNF-Mesenchymal_fibroblastic-Fibroblasts-Diff_MatrixFB\|LPS_IL1RA_TNF / Treatment groups by lineage, cell group, cell type	RPLP1 NR2F1 COL1A1 COL1A2	6.08e-05	198	48	4	0a4b19c3d5e65ecd24fc2ce80ac5276c813282c7
ToppCell	11.5-Airway-Mesenchymal\|Airway / Age, Tissue, Lineage and Cell class	RPLP1 NR2F1 COL1A1 COL1A2	6.08e-05	198	48	4	fe08709d043d927988b1bb262c766b0b572fc927
ToppCell	11.5-Distal-Mesenchymal\|Distal / Age, Tissue, Lineage and Cell class	RPLP1 NR2F1 COL1A1 COL1A2	6.08e-05	198	48	4	5c606d881f151404287d9b43c9490e9bb486ef54
ToppCell	11.5-Airway-Mesenchymal-Mesenchyme_RSPO2+\|Airway / Age, Tissue, Lineage and Cell class	RPLP1 NR2F1 COL1A1 COL1A2	6.08e-05	198	48	4	23783572c22c24d9fb8e14dc1f3852d2094157df
ToppCell	Parenchyma_COVID-19\|World / Sample group, Lineage and Cell type	ARID1B NR2F1 COL1A1 COL1A2	6.08e-05	198	48	4	45ab554e6d0399b3182f089a25b2adf96de1144b
ToppCell	Control_saline-Mesenchymal_fibroblastic-Fibroblasts-Proliferative_MatrixFB\|Control_saline / Treatment groups by lineage, cell group, cell type	RPLP1 NR2F1 COL1A1 COL1A2	6.08e-05	198	48	4	d9d3520705a1142083782f077a0c5604d3ea99af
ToppCell	kidney_cells-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell-parietal_epithelial_cell-Parietal_Epithelial_Cell\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	FOXD2 BHLHE41 FOXD1 COL1A1	6.20e-05	199	48	4	c972d3036151403f26fa9d6271520639c281ab84
ToppCell	11.5-Distal-Mesenchymal-Mesenchyme_RSPO2+\|Distal / Age, Tissue, Lineage and Cell class	RPLP1 NR2F1 COL1A1 COL1A2	6.20e-05	199	48	4	cea1b30f3e3a9b4ccbc8b57f82352067be1a1d68
ToppCell	Tracheal-NucSeq\|Tracheal / Cell types per location group and 10X technology with lineage, and cell group designations	ARID1B PAN3 MAML3 MSI2	6.20e-05	199	48	4	94b94b17ca18b8dc27b91da1f2ccf89e03cc7035
ToppCell	Tracheal-NucSeq-Stromal-Peri/Epineurial_-NAF_epineurial\|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations	FOXD2 NR2F1 FOXD1 COL1A2	6.20e-05	199	48	4	9c2db0bb94cba71a3cc1827844da090e213e0258
ToppCell	18-Distal-Mesenchymal\|Distal / Age, Tissue, Lineage and Cell class	RPLP1 NR2F1 COL1A1 COL1A2	6.20e-05	199	48	4	d65150d2e24c40aa82712e7f034f6772102bd293
ToppCell	kidney_cells-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell-parietal_epithelial_cell\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	FOXD2 BHLHE41 FOXD1 COL1A1	6.20e-05	199	48	4	b9338b739162cd8e5661c9a4dcb41a31219b5723
ToppCell	Tracheal-NucSeq-Stromal-Peri/Epineurial_\|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations	FOXD2 NR2F1 FOXD1 COL1A2	6.20e-05	199	48	4	3835452e4848d7f7dd8651c17b746b271ef39688
ToppCell	LPS_only-Mesenchymal_fibroblastic-Fibroblasts-Diff_MatrixFB\|LPS_only / Treatment groups by lineage, cell group, cell type	RPLP1 NR2F1 COL1A1 COL1A2	6.33e-05	200	48	4	ab4fda0cc95cb8f80ea9f28745013f3248def820
ToppCell	COVID-19-Fibroblasts-Pathological_FB\|COVID-19 / group, cell type (main and fine annotations)	RPLP1 NR2F1 COL1A1 COL1A2	6.33e-05	200	48	4	73e01b7bc43320a991c67a4fd0c04708f893c7ea
ToppCell	Brain_organoid-organoid_Tanaka_cellReport-5w-Neuroepithelial\|5w / Sample Type, Dataset, Time_group, and Cell type.	NR2F1 FOXD1 COL1A1 COL1A2	6.33e-05	200	48	4	69707f9576d326a06faac49701ef5cd632e760f6
ToppCell	Brain_organoid-organoid_Tanaka_cellReport-5w-Neuroepithelial-Proteoglycan-expressing_cell\|5w / Sample Type, Dataset, Time_group, and Cell type.	NR2F1 FOXD1 COL1A1 COL1A2	6.33e-05	200	48	4	f94381d0a3b5b81cdbb13b75fc0e4910cbd70382
ToppCell	COVID-19-lung-Myofibroblast\|lung / Disease (COVID-19 only), tissue and cell type	RPLP1 NR2F1 COL1A1 COL1A2	6.33e-05	200	48	4	3179210cbfa99834bed4db182ce6095a086d64a9
ToppCell	COVID-19-lung-Myofibroblast\|COVID-19 / Disease (COVID-19 only), tissue and cell type	RPLP1 NR2F1 COL1A1 COL1A2	6.33e-05	200	48	4	ccb0fea3fab1227d8c6da7281c1a852c3db42ee9
ToppCell	frontal_cortex-Neuronal-GABAergic_neuron-Sncg-Sncg_Vip_Itih5\|frontal_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	CPNE2 CELF6 DIPK1C	2.52e-04	114	48	3	9f0c8dfd740d50448a6c91a00e7bae4dfc9b3302
ToppCell	Frontal_cortex-Endothelial-ENDOTHELIAL_TIP-Dcn_1-Dcn_1_1\|Frontal_cortex / BrainAtlas - Mouse McCarroll V32	FOXD2 COL1A1 COL1A2	3.62e-04	129	48	3	856255fbfc7f95642000cfd7704141b2388f7c5c
ToppCell	frontal_cortex-Neuronal-GABAergic_neuron-Vip-Vip_Col15a1_Pde1a\|frontal_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	CPNE2 CELF6 DIPK1C	3.71e-04	130	48	3	56b9c3325e011f1dbaf9efc71bd6e1af4f96fda6
ToppCell	Cerebellum-Endothelial-ENDOTHELIAL_TIP-Dcn_1\|Cerebellum / BrainAtlas - Mouse McCarroll V32	FOXD2 GPR88 COL1A1	4.05e-04	134	48	3	d29ac8152dc581c0da2430d06cd259ac0eded808
ToppCell	Cerebellum-Endothelial-ENDOTHELIAL_TIP-Dcn_1-Dcn_1_1\|Cerebellum / BrainAtlas - Mouse McCarroll V32	FOXD2 GPR88 COL1A1	4.05e-04	134	48	3	459c39df15d3cf9144ce7827e8d14830d31353bb
ToppCell	Cerebellum-Endothelial-ENDOTHELIAL_TIP-Dcn_1-Dcn_1_1-Endothelial_Tip.Dcn.Apod_(Apod)-\|Cerebellum / BrainAtlas - Mouse McCarroll V32	FOXD2 GPR88 COL1A1	4.05e-04	134	48	3	d065449ca3679e4818b74fb7302cc7f1ce62f691
ToppCell	Cerebellum-Endothelial-ENDOTHELIAL_TIP-Dcn_1-Dcn_1_1-Endothelial_Tip.Dcn.Apod_(Apod)\|Cerebellum / BrainAtlas - Mouse McCarroll V32	FOXD2 GPR88 COL1A1	4.05e-04	134	48	3	0be389f416818a22e80098dd809fdf45b14171e8
ToppCell	primary_visual_cortex-Non-neuronal-leptomeningeal_cell-VLMC-VLMC_Spp1_Col15a1\|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	FOXD1 COL1A1 COL1A2	4.80e-04	142	48	3	f4e4cde228149d5a536fbf0517ed71d81e296faf
ToppCell	frontal_cortex-Neuronal-GABAergic_neuron-Sncg\|frontal_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	CPNE2 CELF6 DIPK1C	4.80e-04	142	48	3	ed91d2ef4c346f7e1a5402846e2a34cee19c24d1
ToppCell	PCW_05-06-Mesenchymal-Mesenchymal_fibroblastic-mes_immature3_(17)\|PCW_05-06 / Celltypes from embryonic and fetal-stage human lung	NR2F1 COL1A1 COL1A2	5.00e-04	144	48	3	1c001a5a3bbe4ecbce8305f8b260e933033550dd
ToppCell	renal_medulla_nuclei-Renal_AKI_(acute_kidney_injury)-Mesenchymal-Fibroblast-Degenerative_Fibroblast\|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group	CELF6 COL1A1 COL1A2	5.10e-04	145	48	3	07acbf086cffce0628accf078d31bf190f803988
ToppCell	Cerebellum-Endothelial-ENDOTHELIAL_TIP\|Cerebellum / BrainAtlas - Mouse McCarroll V32	FOXD2 FOXD1 COL1A1	5.52e-04	149	48	3	3980fa4f1986a2f164a1826ea043fb71f1d756cd
ToppCell	renal_medulla_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Fibroblast-Collagen-high_Fibroblast-\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	LFNG COL1A1 COL1A2	5.63e-04	150	48	3	1270f33f9d7e46e55adf1a96e8beee858b95589d
ToppCell	renal_medulla_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Fibroblast-Collagen-high_Fibroblast\|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group	LFNG COL1A1 COL1A2	5.63e-04	150	48	3	156118ce1d69522624196410cba18b8354cd0bb4
ToppCell	TCGA-Bladder-Primary_Tumor-Urothelial_Carcinoma-Non-Papillary_Muscle_Invasive_Urothelial_Carcinoma-8\|TCGA-Bladder / Sample_Type by Project: Shred V9	FOXO6 TAF4 MSI2	5.63e-04	150	48	3	1aa9320d97ff10994ea024751790524fe133aba9
ToppCell	TCGA-Thryoid-Primary_Tumor-Thyroid_Papillary_Carcinoma-Tall_Cell-1\|TCGA-Thryoid / Sample_Type by Project: Shred V9	DIPK1C COL1A1 COL1A2	6.31e-04	156	48	3	45a05c7a45a3ec8551818ab67f18b3b9553934c1
Drug	5'-methylthioadenosine	COL1A1 COL1A2	4.35e-06	2	48	2	ctd:C008500
Disease	osteogenesis imperfecta type 3 (is_implicated_in)	COL1A1 COL1A2	2.70e-06	2	49	2	DOID:0110339 (is_implicated_in)
Disease	osteogenesis imperfecta type 4 (is_implicated_in)	COL1A1 COL1A2	2.70e-06	2	49	2	DOID:0110340 (is_implicated_in)
Disease	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE	COL1A1 COL1A2	2.70e-06	2	49	2	C0268345
Disease	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1	COL1A1 COL1A2	2.70e-06	2	49	2	C4551623
Disease	osteogenesis imperfecta type 2 (is_implicated_in)	COL1A1 COL1A2	2.70e-06	2	49	2	DOID:0110341 (is_implicated_in)
Disease	OSTEOGENESIS IMPERFECTA, TYPE IV	COL1A1 COL1A2	2.70e-06	2	49	2	166220
Disease	Osteogenesis imperfecta with normal sclerae, dominant form	COL1A1 COL1A2	2.70e-06	2	49	2	cv:C0268363
Disease	Osteogenesis imperfecta type III	COL1A1 COL1A2	2.70e-06	2	49	2	cv:C0268362
Disease	OSTEOGENESIS IMPERFECTA, TYPE II	COL1A1 COL1A2	2.70e-06	2	49	2	166210
Disease	Osteogenesis imperfecta, perinatal lethal	COL1A1 COL1A2	2.70e-06	2	49	2	cv:C0268358
Disease	OSTEOGENESIS IMPERFECTA, TYPE III	COL1A1 COL1A2	2.70e-06	2	49	2	259420
Disease	osteogenesis imperfecta (is_implicated_in)	COL1A1 COL1A2	8.10e-06	3	49	2	DOID:12347 (is_implicated_in)
Disease	osteogenesis imperfecta type 3 (implicated_via_orthology)	COL1A1 COL1A2	8.10e-06	3	49	2	DOID:0110339 (implicated_via_orthology)
Disease	OSTEOPOROSIS	COL1A1 COL1A2	1.62e-05	4	49	2	166710
Disease	Osteogenesis imperfecta, dominant perinatal lethal	COL1A1 COL1A2	2.69e-05	5	49	2	C0268358
Disease	Lobstein Disease	COL1A1 COL1A2	2.69e-05	5	49	2	C0023931
Disease	osteogenesis imperfecta (implicated_via_orthology)	COL1A1 COL1A2	2.69e-05	5	49	2	DOID:12347 (implicated_via_orthology)
Disease	Ehlers-Danlos Syndrome	COL1A1 COL1A2	2.69e-05	5	49	2	C0013720
Disease	Ehlers-Danlos syndrome (implicated_via_orthology)	COL1A1 COL1A2	4.04e-05	6	49	2	DOID:13359 (implicated_via_orthology)
Disease	Osteoporosis	COL1A1 COL1A2	4.04e-05	6	49	2	cv:C0029456
Disease	Osteogenesis imperfecta type IV (disorder)	COL1A1 COL1A2	1.21e-04	10	49	2	C0268363
Disease	Osteogenesis imperfecta type III (disorder)	COL1A1 COL1A2	1.47e-04	11	49	2	C0268362
Disease	Osteogenesis Imperfecta	COL1A1 COL1A2	2.08e-04	13	49	2	C0029434
Disease	Cardiovascular Abnormalities	ANKS6 ZMIZ1	3.19e-04	16	49	2	C0243050
Disease	Oral Submucous Fibrosis	COL1A1 COL1A2	4.06e-04	18	49	2	C0029172
Disease	Osteogenesis imperfecta	COL1A1 COL1A2	5.56e-04	21	49	2	cv:C0029434
Disease	Liver Cirrhosis	ANKS6 COL1A1 COL1A2	6.77e-04	103	49	3	C0023890
Disease	Fibrosis, Liver	ANKS6 COL1A1 COL1A2	7.16e-04	105	49	3	C0239946
Disease	Heart valve disease	COL1A1 COL1A2	8.56e-04	26	49	2	C0018824
Disease	osteoporosis (is_implicated_in)	COL1A1 COL1A2	1.22e-03	31	49	2	DOID:11476 (is_implicated_in)

Protein segments in the cluster

Peptide	Gene	Start	Entry
APAAAPFVPFSGGGQ	ASPSCR1	236	Q9BZE9
SGGAPAAGAAPMGPQ	CPNE2	6	Q96FN4
GGGGAPFPQPAAAAA	BHLHE41	331	Q9C0J9
PGGGGGPAAVPEFNN	ARID1B	301	Q8NFD5
PVAGAPSVGQPGAGF	SNAP91	826	O60641
GPPRGPAAAAAGYGC	AHDC1	1526	Q5TGY3
AAAAAAAGGPGLPAP	DMRTA2	391	Q96SC8
MAAAPGGSAQPAGPG	CELF6	1	Q96J87
GGFPGANSPGPVADL	MSI2	271	Q96DH6
AAQGNGYAPDGPPGV	ARHGAP39	226	Q9C0H5
AGGNPGGPNPAAQAA	NR2F1	16	P10589
GGAGDPAAAAALFPP	FOXD1	246	Q16676
GAAAGQGAPAPAPAS	LRCH4	466	O75427
AFPGAQHAPGPGGAA	GPR88	246	Q9GZN0
PGEAAVFPQGSGAGP	HELT	161	A6NFD8
GPPGPGAAAAAQQLG	TRIM71	241	Q2Q1W2
AGPAGAAPAPGLGAA	LFNG	46	Q8NES3
AAPAPGLGAAAAAPG	LFNG	51	Q8NES3
GASPAGPGFLGSQPQ	MAML3	721	Q96JK9
GAGPGPAAGAALPDQ	PDCD6	11	O75340
GPYAAAAAGPLGAAP	FOXO6	416	A8MYZ6
PGFGGVPAFGSAPAF	NUP214	1986	P35658
CNVGAGGPAPAAGAA	RPLP1	61	P05386
QPAFGAAEGQPPGAA	POM121C	946	A8CG34
AGAPVAGFPPGAVAG	PAN3	91	Q58A45
EVGPAGPNGFAGPAG	COL1A2	716	P08123
GPNGFAGPAGAAGQP	COL1A2	721	P08123
AGPPGGSSRAAFPQG	CPSF6	186	Q16630
PGAAGGAEDGFFVPP	COPA	896	P53621
GPGAAAAGAVGAPVP	ANKS6	56	Q68DC2
GAPPAQAWAAGPGAG	FIZ1	256	Q96SL8
LAPGGGAAYNLGAPP	MAN2B1	871	O00754
MAAAAAGGAPGPAPG	CABLES2	1	Q9BTV7
FPLDRAPGAPGGGQA	DIPK1C	236	Q0P6D2
GGYGGPAQPPAAAQA	FOSL1	16	P15407
SPGPGAAAARGAAGP	FOXD2	96	O60548
GPPFAAAAGPGGQAQ	FOXD2	436	O60548
PGAEGNAPAPGAGGQ	KIF13B	1671	Q9NQT8
AGAGPAAPAEGAPGA	TAF4	71	O00268
GGSAGAAPAPAPAAG	TAF4	306	O00268
ACFKGGAGGPAAPAP	SCRT1	326	Q9BWW7
VGAAGAEPPNAGDPF	NKX1-1	146	Q15270
QDTPAFGPALPAGGG	SIPA1	481	Q96FS4
FGPALPAGGGPFAAN	SIPA1	486	Q96FS4
AGFAGAAGGPSPVAA	PTGES2	36	Q9H7Z7
APGFPAGAQGSGLPA	PROB1	636	E7EW31
GLQVGPPAGSPFGAA	SMARCD2	86	Q92925
AAGPAGNPGADGQPG	COL1A1	381	P02452
AGFAGPPGADGQPGA	COL1A1	811	P02452
GSAGPPGATGFPGAA	COL1A1	866	P02452
AGGGAPVAVAGAPVF	SPEG	31	Q15772
PAGDGGPGAPARYAN	SNX18	66	Q96RF0
APPAGYGAQPVGNEG	WBP2NL	191	Q6ICG8
AASFPGGPEFPQGRG	TPRX2	106	P0DV77
GASYPGGPNAPAGMG	ZMIZ1	251	Q9ULJ6
GGPAAQAAPAAPGLS	TTF2	326	Q9UNY4