Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionG protein-coupled photoreceptor activity

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

7.40e-0815564GO:0008020
GeneOntologyMolecularFunctionphotoreceptor activity

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

1.28e-0717564GO:0009881
GeneOntologyMolecularFunctionthreonine-tRNA ligase activity

TARS3 TARS1

2.31e-053562GO:0004829
GeneOntologyMolecularFunctionhexosyltransferase activity

POMT2 B4GAT1 AGL B4GALNT3 GALNT13 LARGE1

2.71e-05211566GO:0016758
GeneOntologyMolecularFunctionglycosyltransferase activity

POMT2 B4GAT1 AGL B4GALNT3 GALNT13 LARGE1

1.51e-04288566GO:0016757
GeneOntologyMolecularFunctionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen

KDM5B KDM2A NOS1 CYP4F11 HIF1AN

2.10e-04194565GO:0016705
GeneOntologyMolecularFunctionligase activity, forming carbon-oxygen bonds

TARS3 VARS1 TARS1

2.22e-0442563GO:0016875
GeneOntologyMolecularFunctionaminoacyl-tRNA ligase activity

TARS3 VARS1 TARS1

2.22e-0442563GO:0004812
GeneOntologyMolecularFunctiontransition metal ion binding

BMP1 KDM5B SF3A3 KDM2A CPZ ACE NOS1 CYP4F11 HIF1AN TARS1 LARGE1

3.98e-0411895611GO:0046914
GeneOntologyMolecularFunctionzinc ion binding

BMP1 KDM5B SF3A3 KDM2A CPZ ACE NOS1 HIF1AN TARS1

7.73e-04891569GO:0008270
GeneOntologyMolecularFunction2-oxoglutarate-dependent dioxygenase activity

KDM5B KDM2A HIF1AN

8.07e-0465563GO:0016706
GeneOntologyMolecularFunctionUDP-glycosyltransferase activity

B4GAT1 B4GALNT3 GALNT13 LARGE1

8.93e-04153564GO:0008194
GeneOntologyMolecularFunctiontransmembrane transporter binding

NEDD4L CNTNAP2 TSPO NOS1

1.38e-03172564GO:0044325
GeneOntologyMolecularFunctioncysteine-type endopeptidase activity

TINAG CTSH CTSW

1.81e-0386563GO:0004197
GeneOntologyMolecularFunctionflavin adenine dinucleotide binding

DMGDH TXNRD2 NOS1

2.34e-0394563GO:0050660
GeneOntologyMolecularFunctiondioxygenase activity

KDM5B KDM2A HIF1AN

2.63e-0398563GO:0051213
GeneOntologyMolecularFunctionhistone H3 demethylase activity

KDM5B KDM2A

2.79e-0328562GO:0141052
GeneOntologyMolecularFunctionhistone demethylase activity

KDM5B KDM2A

3.41e-0331562GO:0032452
GeneOntologyMolecularFunctionprotein demethylase activity

KDM5B KDM2A

3.63e-0332562GO:0140457
GeneOntologyMolecularFunctionexopeptidase activity

CPZ ACE CTSH

3.65e-03110563GO:0008238
GeneOntologyMolecularFunctionacetylgalactosaminyltransferase activity

B4GALNT3 GALNT13

4.33e-0335562GO:0008376
GeneOntologyMolecularFunctionglucuronosyltransferase activity

B4GAT1 LARGE1

4.33e-0335562GO:0015020
GeneOntologyMolecularFunctioncarboxylic acid binding

DMGDH NOS1 CYP4F11 HIF1AN

4.52e-03239564GO:0031406
GeneOntologyMolecularFunctionoxidoreductase activity

DMGDH KDM5B KDM2A TXNRD2 NOS1 CYP4F11 HIF1AN

5.38e-03766567GO:0016491
GeneOntologyMolecularFunctionorganic acid binding

DMGDH NOS1 CYP4F11 HIF1AN

5.59e-03254564GO:0043177
GeneOntologyMolecularFunctionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen

NOS1 CYP4F11

5.63e-0340562GO:0016709
GeneOntologyMolecularFunctiondemethylase activity

KDM5B KDM2A

6.78e-0344562GO:0032451
GeneOntologyMolecularFunctionsodium channel regulator activity

NEDD4L NOS1

6.78e-0344562GO:0017080
GeneOntologyMolecularFunctionendopeptidase activity

BMP1 TINAG ACE CTSH CTSW

7.02e-03430565GO:0004175
GeneOntologyMolecularFunctionacetylglucosaminyltransferase activity

B4GAT1 LARGE1

7.70e-0347562GO:0008375
GeneOntologyMolecularFunctioncatalytic activity, acting on a tRNA

TARS3 VARS1 TARS1

7.70e-03144563GO:0140101
GeneOntologyMolecularFunctioncarboxypeptidase activity

CPZ ACE

8.35e-0349562GO:0004180
GeneOntologyBiologicalProcessphototransduction

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

1.12e-0553544GO:0007602
GeneOntologyBiologicalProcessdetection of visible light

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

1.50e-0557544GO:0009584
GeneOntologyBiologicalProcessprotein O-linked mannosylation

POMT2 B4GAT1 LARGE1

1.60e-0519543GO:0035269
GeneOntologyBiologicalProcessthreonyl-tRNA aminoacylation

TARS3 TARS1

2.01e-053542GO:0006435
GeneOntologyBiologicalProcessresponse to abiotic stimulus

OPN1MW2 TGFB2 OPN1MW3 DRD5 NEDD4L CNTNAP2 TSPO OPN1LW TXNRD2 OPN1MW ACE NOS1 LARGE1

3.68e-0513615413GO:0009628
GeneOntologyBiologicalProcessprotein mannosylation

POMT2 B4GAT1 LARGE1

3.75e-0525543GO:0035268
GeneOntologyBiologicalProcessmannosylation

POMT2 B4GAT1 LARGE1

4.23e-0526543GO:0097502
GeneOntologyBiologicalProcessdetection of light stimulus

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

4.93e-0577544GO:0009583
GeneOntologyBiologicalProcessresponse to light stimulus

OPN1MW2 OPN1MW3 DRD5 CNTNAP2 OPN1LW OPN1MW LARGE1

5.92e-05382547GO:0009416
GeneOntologyBiologicalProcessneuropeptide catabolic process

ACE CTSH

6.69e-055542GO:0010813
GeneOntologyBiologicalProcessnegative regulation of monoatomic ion transport

TGFB2 NEDD4L BEST3 ACE NOS1

8.41e-05171545GO:0043271
GeneOntologyBiologicalProcessmotor behavior

NAGLU CNTNAP2 MFSD8

1.05e-0435543GO:0061744
GeneOntologyBiologicalProcessglycoprotein metabolic process

POMT2 SULF2 B4GAT1 NAGLU MFSD8 GALNT13 LARGE1

1.24e-04430547GO:0009100
GeneOntologyBiologicalProcessbradykinin catabolic process

ACE CTSH

1.40e-047542GO:0010815
GeneOntologyBiologicalProcessreactive gliosis

POMT2 LARGE1

1.40e-047542GO:0150103
GeneOntologyBiologicalProcesspositive regulation of cell division

OPN1MW2 TGFB2 OPN1LW OPN1MW

1.59e-04104544GO:0051781
GeneOntologyBiologicalProcessprotein O-linked glycosylation

POMT2 B4GAT1 GALNT13 LARGE1

1.65e-04105544GO:0006493
GeneOntologyBiologicalProcesstRNA aminoacylation for protein translation

TARS3 VARS1 TARS1

1.81e-0442543GO:0006418
GeneOntologyBiologicalProcesstRNA aminoacylation

TARS3 VARS1 TARS1

2.23e-0445543GO:0043039
GeneOntologyBiologicalProcessamino acid activation

TARS3 VARS1 TARS1

2.38e-0446543GO:0043038
GeneOntologyBiologicalProcessregulation of gap junction assembly

CNTNAP2 ACE

2.99e-0410542GO:1903596
GeneOntologyBiologicalProcessendocrine process

KDM5B DRD5 TSPO ACE

3.02e-04123544GO:0050886
GeneOntologyBiologicalProcessresponse to radiation

OPN1MW2 OPN1MW3 DRD5 CNTNAP2 OPN1LW OPN1MW LARGE1

3.23e-04503547GO:0009314
GeneOntologyBiologicalProcessmulticellular organismal response to stress

CNTNAP2 TSPO NOS1 LARGE1

3.32e-04126544GO:0033555
GeneOntologyBiologicalProcesscellular response to light stimulus

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

3.73e-04130544GO:0071482
GeneOntologyBiologicalProcessdetermination of adult lifespan

NAGLU MFSD8 LARGE1

3.83e-0454543GO:0008340
GeneOntologyBiologicalProcesspositive regulation of cytokinesis

OPN1MW2 OPN1LW OPN1MW

4.04e-0455543GO:0032467
GeneOntologyBiologicalProcesscellular response to abiotic stimulus

OPN1MW2 OPN1MW3 TSPO OPN1LW OPN1MW NOS1

4.06e-04371546GO:0071214
GeneOntologyBiologicalProcesscellular response to environmental stimulus

OPN1MW2 OPN1MW3 TSPO OPN1LW OPN1MW NOS1

4.06e-04371546GO:0104004
GeneOntologyCellularComponentphotoreceptor disc membrane

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

7.10e-0726574GO:0097381
GeneOntologyCellularComponentnon-motile cilium

OPN1MW2 OPN1MW3 DRD5 OPN1LW OPN1MW

1.94e-04196575GO:0097730
GeneOntologyCellularComponentphotoreceptor outer segment

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

2.39e-04111574GO:0001750
GeneOntologyCellularComponentphotoreceptor cell cilium

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

5.63e-04139574GO:0097733
GeneOntologyCellularComponent9+0 non-motile cilium

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

8.06e-04153574GO:0097731
HumanPhenoRed-green dyschromatopsia

OPN1LW MFSD8 OPN1MW

1.68e-0511253HP:0000642
HumanPhenoBlue cone monochromacy

OPN1LW OPN1MW

2.31e-052252HP:0007939
HumanPhenoCone monochromacy

OPN1LW OPN1MW

2.31e-052252HP:0011517
HumanPhenoType II lissencephaly

POMT2 B4GAT1 LARGE1

5.61e-0516253HP:0007260
HumanPhenoReduced OCT-measured foveal thickness

OPN1LW OPN1MW

6.92e-053252HP:0030619
HumanPhenoChorioretinal dysplasia

POMT2 B4GAT1 LARGE1

1.31e-0421253HP:0007731
HumanPhenoAbnormal OCT-measured foveal thickness

OPN1LW OPN1MW

1.38e-044252HP:0030617
HumanPhenoMetatarsus valgus

POMT2 B4GAT1 LARGE1

1.51e-0422253HP:0010508
HumanPhenoMyopia

POMT2 KDM5B NEDD4L OPN1LW MFSD8 OPN1MW VARS1 TARS1 LARGE1

1.62e-04447259HP:0000545
HumanPhenoMeningoencephalocele

POMT2 LARGE1

2.29e-045252HP:0006888
HumanPhenoAbnormality of the tongue muscle

POMT2 LARGE1

2.29e-045252HP:0040173
HumanPhenoRetinal dysplasia

POMT2 B4GAT1 LARGE1

2.52e-0426253HP:0007973
HumanPhenoAbnormal circulating aldolase concentration

POMT2 B4GAT1 LARGE1

2.52e-0426253HP:0012400
HumanPhenoKinked brainstem

POMT2 LARGE1

3.43e-046252HP:0012793
DomainOpsin_red/grn

OPN1MW3 OPN1LW OPN1MW

2.16e-083533IPR000378
DomainPept_asp_AS

TINAG CTSH CTSW

2.55e-0610533IPR025661
DomainOPSIN

OPN1MW3 OPN1LW OPN1MW

2.55e-0610533PS00238
DomainOpsin

OPN1MW3 OPN1LW OPN1MW

3.50e-0611533IPR001760
DomainPept_C1

TINAG CTSH CTSW

6.05e-0613533SM00645
DomainPeptidase_C1A_C

TINAG CTSH CTSW

6.05e-0613533IPR000668
DomainPeptidase_C1

TINAG CTSH CTSW

6.05e-0613533PF00112
DomainPeptidase_C1A

TINAG CTSH CTSW

6.05e-0613533IPR013128
DomainThrRS_core

TARS3 TARS1

2.37e-053532IPR033728
DomainThr-tRNA-ligase_IIa

TARS3 TARS1

2.37e-053532IPR002320
DomainZinc_finger_PHD-type_CS

KDM5B PHF20 KDM2A NSD3

3.44e-0565534IPR019786
DomainTHIOL_PROTEASE_ASN

TINAG CTSH CTSW

6.01e-0527533PS00640
DomainPept_cys_AS

TINAG CTSH CTSW

6.72e-0528533IPR000169
DomainZnf_PHD-finger

KDM5B PHF20 KDM2A NSD3

7.42e-0579534IPR019787
DomainJMJC

KDM5B KDM2A HIF1AN

1.01e-0432533PS51184
DomainJmjC_dom

KDM5B KDM2A HIF1AN

1.01e-0432533IPR003347
DomainJmjC

KDM5B KDM2A HIF1AN

1.11e-0433533SM00558
DomainTGS

TARS3 TARS1

1.18e-046532IPR004095
DomainTGS

TARS3 TARS1

1.18e-046532PF02824
DomainPHD

KDM5B PHF20 KDM2A NSD3

1.18e-0489534SM00249
DomainZnf_PHD

KDM5B PHF20 KDM2A NSD3

1.29e-0491534IPR001965
DomainZF_PHD_2

KDM5B PHF20 KDM2A NSD3

1.52e-0495534PS50016
DomainZF_PHD_1

KDM5B PHF20 KDM2A NSD3

1.58e-0496534PS01359
DomainInhibitor_I29

CTSH CTSW

1.64e-047532PF08246
DomainProt_inhib_I29

CTSH CTSW

1.64e-047532IPR013201
DomainTGS-like

TARS3 TARS1

1.64e-047532IPR012676
DomaintRNA_SAD

TARS3 TARS1

1.64e-047532SM00863
DomainInhibitor_I29

CTSH CTSW

1.64e-047532SM00848
DomaintRNA_SAD

TARS3 TARS1

1.64e-047532IPR012947
DomaintRNA_SAD

TARS3 TARS1

1.64e-047532PF07973
DomainThr/Ala-tRNA-synth_IIc_edit

TARS3 TARS1

2.19e-048532IPR018163
DomainHGTP_anticodon

TARS3 TARS1

2.81e-049532PF03129
DomainPept_his_AS

CTSH CTSW

4.27e-0411532IPR025660
Domainaa-tRNA-synt_IIb

TARS3 TARS1

4.27e-0411532IPR002314
DomaintRNA-synt_2b

TARS3 TARS1

4.27e-0411532PF00587
Domain-

TARS3 TARS1

4.27e-04115323.40.50.800
DomainBeta-grasp_dom

TARS3 TARS1

7.03e-0414532IPR012675
Domain-

TARS3 TARS1

7.03e-04145323.10.20.30
DomainAnticodon-bd

TARS3 TARS1

7.03e-0414532IPR004154
DomainZnf_FYVE_PHD

KDM5B PHF20 KDM2A NSD3

8.00e-04147534IPR011011
Domainaa-tRNA-synth_II

TARS3 TARS1

1.17e-0318532IPR006195
DomainAA_TRNA_LIGASE_II

TARS3 TARS1

1.17e-0318532PS50862
DomainPHD

KDM5B PHF20 NSD3

1.26e-0375533PF00628
Domain-

B4GALNT3 GALNT13 LARGE1

1.57e-03815333.90.550.10
DomainNucleotide-diphossugar_trans

B4GALNT3 GALNT13 LARGE1

2.00e-0388533IPR029044
DomainJmjC

KDM5B KDM2A

2.10e-0324532PF02373
DomainTHIOL_PROTEASE_CYS

CTSH CTSW

2.46e-0326532PS00139
DomainTHIOL_PROTEASE_HIS

CTSH CTSW

2.65e-0327532PS00639
DomainTGF-beta-rel

TGFB2 BMP15

3.71e-0332532IPR015615
DomainFIBRINOGEN_C_1

TNN CNTNAP2

3.71e-0332532PS00514
DomainFibrinogen_a/b/g_C_dom

TNN CNTNAP2

3.71e-0332532IPR002181
DomainFIBRINOGEN_C_2

TNN CNTNAP2

3.71e-0332532PS51406
DomainTGFb_CS

TGFB2 BMP15

3.71e-0332532IPR017948
DomainTGFB

TGFB2 BMP15

4.94e-0337532SM00204
DomainTGF-b_C

TGFB2 BMP15

4.94e-0337532IPR001839
DomainTGF_BETA_2

TGFB2 BMP15

4.94e-0337532PS51362
DomainTGF_beta

TGFB2 BMP15

4.94e-0337532PF00019
DomainTGF_BETA_1

TGFB2 BMP15

4.94e-0337532PS00250
PathwayREACTOME_THE_RETINOID_CYCLE_IN_CONES_DAYLIGHT_VISION

OPN1MW2 OPN1MW3 OPN1LW

1.80e-068463MM14880
PathwayREACTOME_OPSINS

OPN1MW2 OPN1MW3 OPN1LW

3.84e-0610463MM15063
PathwayKEGG_MEDICUS_REFERENCE_MANNOSE_TYPE_O_GLYCAN_BIOSYNTHESIS_FKTN_TO_LARGE

B4GAT1 LARGE1

1.55e-046462M47618
PathwayREACTOME_THE_RETINOID_CYCLE_IN_CONES_DAYLIGHT_VISION

OPN1LW OPN1MW

2.16e-047462M27157
PathwayKEGG_AMINOACYL_TRNA_BIOSYNTHESIS

TARS3 VARS1 TARS1

3.18e-0441463M14691
PathwayREACTOME_OPSINS

OPN1LW OPN1MW

3.70e-049462M6285
PathwayREACTOME_O_LINKED_GLYCOSYLATION

POMT2 B4GAT1 GALNT13 LARGE1

4.30e-04109464MM15164
PathwayREACTOME_O_LINKED_GLYCOSYLATION

POMT2 B4GAT1 GALNT13 LARGE1

4.61e-04111464M27416
PathwayKEGG_LYSOSOME

NAGLU MFSD8 CTSH CTSW

6.38e-04121464M11266
PathwayREACTOME_RETINOID_CYCLE_DISEASE_EVENTS

OPN1LW OPN1MW

7.94e-0413462M29612
PathwayKEGG_GLYCOSAMINOGLYCAN_BIOSYNTHESIS_KERATAN_SULFATE

B4GAT1 CHST2

1.06e-0315462M3042
PathwaySA_MMP_CYTOKINE_CONNECTION

TGFB2 ACE

1.06e-0315462M11736
Pubmed

Human L- and M-opsins restore M-cone function in a mouse model for human blue cone monochromacy.

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

6.48e-12457429386880
Pubmed

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

3.24e-1155742937147
Pubmed

Molecular determinants of human red/green color discrimination.

OPN1MW2 OPN1LW OPN1MW

4.17e-0935738185948
Pubmed

X-linked cone dystrophy caused by mutation of the red and green cone opsins.

OPN1MW2 OPN1LW OPN1MW

4.17e-09357320579627
Pubmed

Expression of red/green-cone opsin mutants K82E, P187S, M273K result in unique pathobiological perturbations to cone structure and function.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357338410159
Pubmed

Chloride-dependent spectral tuning mechanism of L-group cone visual pigments.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357323350963
Pubmed

Distinct contributions of rod, cone, and melanopsin photoreceptors to encoding irradiance.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357320471354
Pubmed

Multiple hypothalamic cell populations encoding distinct visual information.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357321224225
Pubmed

Circadian Regulation of the Rod Contribution to Mesopic Vision in Mice.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357336216501
Pubmed

Spectral tuning of a circadian photopigment in a subterranean 'blind' mammal (Spalax ehrenbergi).

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357310567724
Pubmed

Extensive cone-dependent spectral opponency within a discrete zone of the lateral geniculate nucleus supporting mouse color vision.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357334111401
Pubmed

Genetically engineered mice with an additional class of cone photoreceptors: implications for the evolution of color vision.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357314500905
Pubmed

Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357328751656
Pubmed

Rescue of M-cone Function in Aged Opn1mw-/- Mice, a Model for Late-Stage Blue Cone Monochromacy.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357331469404
Pubmed

The molecular genetics and evolution of red and green color vision in vertebrates.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357311545071
Pubmed

Mechanisms of spectral tuning in the mouse green cone pigment.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-0935739238068
Pubmed

Emergence of novel color vision in mice engineered to express a human cone photopigment.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357317379811
Pubmed

Co-expression of murine opsins facilitates identifying the site of cone adaptation.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-09357312511072
Pubmed

The Pem homeobox gene is X-linked and exclusively expressed in extraembryonic tissues during early murine development.

OPN1MW2 OPN1MW3 OPN1LW

4.17e-0935737958444
Pubmed

Visual responses in the dorsal lateral geniculate nucleus at early stages of retinal degeneration in rd1 PDE6β mice.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457331461375
Pubmed

Murine and bovine blue cone pigment genes: cloning and characterization of two new members of the S family of visual pigments.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-0845738088841
Pubmed

Modulation of Fast Narrowband Oscillations in the Mouse Retina and dLGN According to Background Light Intensity.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457328103478
Pubmed

Molecular biology of the visual pigments.

OPN1MW2 OPN1LW OPN1MW

1.67e-0845733303660
Pubmed

Cones Support Alignment to an Inconsistent World by Suppressing Mouse Circadian Responses to the Blue Colors Associated with Twilight.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457331846668
Pubmed

Melanopsin-driven increases in maintained activity enhance thalamic visual response reliability across a simulated dawn.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457326438865
Pubmed

Light/dark translocation of alphatransducin in mouse photoreceptor cells expressing G90D mutant opsin.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457317249565
Pubmed

Structural and functional rescue of cones carrying the most common cone opsin C203R missense mutation.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457338060327
Pubmed

Contribution of M-opsin-based color vision to refractive development in mice.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457334126082
Pubmed

Physiological features of the S- and M-cone photoreceptors of wild-type mice from single-cell recordings.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457316567464
Pubmed

S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variant.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457324801621
Pubmed

Melanopsin Contributions to the Representation of Images in the Early Visual System.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457328528909
Pubmed

Melanopsin-driven light adaptation in mouse vision.

OPN1MW2 OPN1MW3 OPN1LW

1.67e-08457325308073
Pubmed

Noncoding Mutations in a Thyroid Hormone Receptor Gene That Impair Cone Photoreceptor Function.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557336631163
Pubmed

Using Silent Substitution to Track the Mesopic Transition From Rod- to Cone-Based Vision in Mice.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557326818794
Pubmed

A common integration locus in type B retrovirus-induced thymic lymphomas.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-0855731333116
Pubmed

A distinct contribution of short-wavelength-sensitive cones to light-evoked activity in the mouse pretectal olivary nucleus.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557322090509
Pubmed

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557310723722
Pubmed

Peripherin-2 differentially interacts with cone opsins in outer segments of cone photoreceptors.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557327033727
Pubmed

Melanopsin-based brightness discrimination in mice and humans.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557322633808
Pubmed

The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557311055434
Pubmed

Enhancer/promoter activities of the long/middle wavelength-sensitive opsins of vertebrates mediated by thyroid hormone receptor β2 and COUP-TFII.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557324058409
Pubmed

Variations in photoreceptor throughput to mouse visual cortex and the unique effects on tuning.

OPN1MW2 OPN1MW3 OPN1LW

4.16e-08557334099749
Pubmed

Functional comparison of rod and cone Gα(t) on the regulation of light sensitivity.

OPN1MW2 OPN1MW3 OPN1LW

8.32e-08657323288843
Pubmed

Reduced levels of dystrophin associated proteins in the brains of mice deficient for Dp71.

OPN1MW2 OPN1MW3 OPN1LW

8.32e-0865738872469
Pubmed

A thyroid hormone receptor that is required for the development of green cone photoreceptors.

OPN1MW2 OPN1MW3 OPN1LW

8.32e-08657311138006
Pubmed

Impaired cytokine signaling in mice lacking the IL-1 receptor-associated kinase.

OPN1MW2 OPN1MW3 OPN1LW

8.32e-08657310395695
Pubmed

Transient expression of thyroid hormone nuclear receptor TRbeta2 sets S opsin patterning during cone photoreceptor genesis.

OPN1MW2 OPN1MW3 OPN1LW

8.32e-08657317436273
Pubmed

Telomere-related markers for the pseudoautosomal region of the mouse genome.

OPN1MW2 OPN1MW3 OPN1LW

8.32e-0865731549575
Pubmed

Retarded developmental expression and patterning of retinal cone opsins in hypothyroid mice.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-07757318974269
Pubmed

Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-0775738001979
Pubmed

NeuroD1 regulates expression of thyroid hormone receptor 2 and cone opsins in the developing mouse retina.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-07757318199774
Pubmed

Mapping of the murine tbl1 gene reveals a new rearrangement between mouse and human X Chromosomes.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-0775739880679
Pubmed

Characterization of cDNAs encoding the murine interleukin 2 receptor (IL-2R) gamma chain: chromosomal mapping and tissue specificity of IL-2R gamma chain expression.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-0775738378320
Pubmed

Rod Photoreceptor Activation Alone Defines the Release of Dopamine in the Retina.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-07757330799247
Pubmed

Activation of the blue opsin gene in cone photoreceptor development by retinoid-related orphan receptor beta.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-07757316574740
Pubmed

Rods progressively escape saturation to drive visual responses in daylight conditions.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-07757329180667
Pubmed

Cloning and distribution of myosin 3B in the mouse retina: differential distribution in cone outer segments.

OPN1MW2 OPN1MW3 OPN1LW

1.45e-07757319332056
Pubmed

Localization of the mdx mutation within the mouse dystrophin gene.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-0785732903046
Pubmed

Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromes.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-0785731572654
Pubmed

Two transcription factors can direct three photoreceptor outcomes from rod precursor cells in mouse retinal development.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-07857321813673
Pubmed

X-chromosome gene order in different Mus species crosses.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-0785733416629
Pubmed

The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-07857312651948
Pubmed

Transcriptional profiling of murine retinas undergoing semi-synchronous cone photoreceptor differentiation.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-07857331163126
Pubmed

Type 3 deiodinase, a thyroid-hormone-inactivating enzyme, controls survival and maturation of cone photoreceptors.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-07857320203194
Pubmed

Tubby is required for trafficking G protein-coupled receptors to neuronal cilia.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-07857323351594
Pubmed

A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3).

OPN1MW2 OPN1MW3 OPN1LW

2.32e-07857310725384
Pubmed

Retinoid X receptor (gamma) is necessary to establish the S-opsin gradient in cone photoreceptors of the developing mouse retina.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-07857316043864
Pubmed

Nr2e3 functional domain ablation by CRISPR-Cas9D10A identifies a new isoform and generates retinitis pigmentosa and enhanced S-cone syndrome models.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-07857333007388
Pubmed

Linkage of amelogenin (Amel) to the distal portion of the mouse X chromosome.

OPN1MW2 OPN1MW3 OPN1LW

2.32e-0785731675194
Pubmed

Retinal dystrophy resulting from ablation of RXR alpha in the mouse retinal pigment epithelium.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-07957314742273
Pubmed

Feedback induction of a photoreceptor-specific isoform of retinoid-related orphan nuclear receptor β by the rod transcription factor NRL.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-07957325296752
Pubmed

Comparative mapping of the actin-binding protein 280 genes in human and mouse.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-0795738088838
Pubmed

ZBED4, a cone and Müller cell protein in human retina, has a different cellular expression in mouse.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-07957321850176
Pubmed

Top2b is involved in the formation of outer segment and synapse during late-stage photoreceptor differentiation by controlling key genes of photoreceptor transcriptional regulatory network.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-07957328370415
Pubmed

IFT20 is required for opsin trafficking and photoreceptor outer segment development.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-07957321307337
Pubmed

Multilocus molecular mapping of the mouse X chromosome.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-0795732906327
Pubmed

A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-07957327669145
Pubmed

Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-0795731973136
Pubmed

Distinct functions of photoreceptor cell-specific nuclear receptor, thyroid hormone receptor beta2 and CRX in one photoreceptor development.

OPN1MW2 OPN1MW3 OPN1LW

3.48e-07957312407160
Pubmed

Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3.

OPN1MW2 OPN1MW3 OPN1LW

4.97e-07105731349842
Pubmed

Cyclophilin-related protein RanBP2 acts as chaperone for red/green opsin.

OPN1MW2 OPN1LW OPN1MW

4.97e-07105738857542
Pubmed

Linkage of a gene for neural cell adhesion molecule, L1 (CamL1) to the Rsvp region of the mouse X chromosome.

OPN1MW2 OPN1MW3 OPN1LW

4.97e-07105731964443
Pubmed

Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye.

OPN1MW2 OPN1MW3 OPN1LW

4.97e-071057321148184
Pubmed

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function.

OPN1MW2 OPN1MW3 OPN1LW

4.97e-071057331949211
Pubmed

Comparative mapping on the mouse and human X chromosomes of a human cDNA clone encoding the vasopressin renal-type receptor (AVP2R).

OPN1MW2 OPN1MW3 OPN1LW

4.97e-07105738449515
Pubmed

The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification.

OPN1MW2 OPN1MW3 OPN1LW

4.97e-071057332236127
Pubmed

Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28.

OPN1MW2 OPN1MW3 OPN1LW

4.97e-07105731684949
Pubmed

Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome.

OPN1MW2 OPN1MW3 OPN1LW

4.97e-07105731973380
Pubmed

Physical linkage of the A-raf-1, properdin, synapsin I, and TIMP genes on the human and mouse X chromosomes.

OPN1MW2 OPN1MW3 OPN1LW

6.82e-07115731572636
Pubmed

Mannose supplements induce embryonic lethality and blindness in phosphomannose isomerase hypomorphic mice.

OPN1MW2 OPN1MW3 OPN1LW

6.82e-071157324421398
Pubmed

Mapping of the glycine receptor alpha 2-subunit gene and the GABAA alpha 3-subunit gene on the mouse X chromosome.

OPN1MW2 OPN1MW3 OPN1LW

9.09e-07125731679744
Pubmed

The spatial patterning of mouse cone opsin expression is regulated by bone morphogenetic protein signaling through downstream effector COUP-TF nuclear receptors.

OPN1MW2 OPN1MW3 OPN1LW

9.09e-071257319812316
Pubmed

MAP4K4 is involved in the neuronal development of retinal photoreceptors.

OPN1MW2 OPN1MW3 OPN1LW

9.09e-071257337290629
Pubmed

AGO61-dependent GlcNAc modification primes the formation of functional glycans on α-dystroglycan.

POMT2 B4GAT1 LARGE1

9.09e-071257324256719
Pubmed

Genetic and physical mapping of the biglycan gene on the mouse X chromosome.

OPN1MW2 OPN1MW3 OPN1LW

9.09e-07125738093671
Pubmed

The construction of human somatic cell hybrids containing portions of the mouse X chromosome and their use to generate DNA probes via interspersed repetitive sequence polymerase chain reaction.

OPN1MW2 OPN1MW3 OPN1LW

9.09e-07125731916827
Pubmed

Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease.

OPN1MW2 OPN1MW3 OPN1LW

9.09e-07125732561974
Pubmed

The expression analysis of Sfrs10 and Celf4 during mouse retinal development.

OPN1MW2 OPN1MW3 OPN1LW

1.18e-061357323932931
Pubmed

Essential functions of synapsins I and II in synaptic vesicle regulation.

OPN1MW2 OPN1MW3 OPN1LW

1.18e-06135737777057
Pubmed

G protein-coupled receptors participate in cytokinesis.

OPN1MW2 OPN1LW OPN1MW

1.18e-061357322888021
CytobandEnsembl 112 genes in cytogenetic band chrXq28

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

1.47e-04213574chrXq28
CytobandXq28

OPN1MW2 OPN1LW OPN1MW

1.39e-03176573Xq28
Cytoband11q13.2

B4GAT1 KDM2A

1.58e-034757211q13.2
Cytoband4p16.1

DRD5 CPZ

4.39e-03795724p16.1
GeneFamilyOpsin receptors

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

5.42e-0911384215
GeneFamilyPHD finger proteins

KDM5B PHF20 KDM2A NSD3

3.72e-059038488
GeneFamilyBone morphogenetic proteins|Astacins

BMP1 BMP15

2.34e-0411382455
GeneFamilyCathepsins

CTSH CTSW

4.44e-0415382470
GeneFamilyPHD finger proteins|Lysine demethylases

KDM5B KDM2A

1.15e-0324382485
CoexpressionNABA_MATRISOME

TGFB2 BMP1 TINAG SULF2 TNN CTSH CRISPLD1 CTSW TGM5 BMP15

4.10e-0510085510MM17056
CoexpressionNABA_MATRISOME

TGFB2 BMP1 TINAG SULF2 TNN CTSH CRISPLD1 CTSW TGM5 BMP15

4.76e-0510265510M5889
CoexpressionGSE22935_WT_VS_MYD88_KO_MACROPHAGE_48H_MBOVIS_BCG_STIM_UP

TARS3 NEDD4L CCSER2 NOS1 HIF1AN

6.13e-05199555M7766
CoexpressionGSE360_L_DONOVANI_VS_L_MAJOR_DC_UP

PHF20 NEDD4L TNN CCSER2 LARGE1

6.28e-05200555M5192
CoexpressionGSE19888_CTRL_VS_TCELL_MEMBRANES_ACT_MAST_CELL_PRETREAT_A3R_INH_UP

TARS3 TINAG AGL BTNL9 CRISPLD1

6.28e-05200555M7335
CoexpressionAtlasDevelopingKidney_e15.5_early proxim tubul_emap-28005_k-means-cluster#5_top-relative-expression-ranked_1000

DMGDH TINAG ELOVL1 TSPO ACE CTSH

2.03e-05230526gudmap_developingKidney_e15.5_early proxim tubul_1000_k5
ToppCellBrain_organoid-organoid_Tanaka_cellReport-2m-Neuronal-Intermediate|2m / Sample Type, Dataset, Time_group, and Cell type.

KDM5B NEDD4L CCSER2 CNTNAP2 TARS1 NSD3

1.93e-072005662a635694844ddabcd98462c5636a6f41a3f08a46
ToppCellGlobus_pallidus-Endothelial-ENDOTHELIAL_STALK-Flt1_1-Endothelial_Stalk.Flt1.Apold1_(Pi16)|Globus_pallidus / BrainAtlas - Mouse McCarroll V32

DMGDH GVINP1 CTSW BMP15

3.17e-06805648713818f57f40c07268f791b45c8af6d522c628f
ToppCellGlobus_pallidus-Endothelial-ENDOTHELIAL_STALK-Flt1_1-Endothelial_Stalk.Flt1.Apold1_(Pi16)--|Globus_pallidus / BrainAtlas - Mouse McCarroll V32

DMGDH GVINP1 CTSW BMP15

3.17e-0680564475e1595528aef08799f099d7dc54412eaa14742
ToppCellGlobus_pallidus-Endothelial-ENDOTHELIAL_STALK-Flt1_1-Endothelial_Stalk.Flt1.Apold1_(Pi16)-|Globus_pallidus / BrainAtlas - Mouse McCarroll V32

DMGDH GVINP1 CTSW BMP15

3.17e-068056409baf1f1a4f07369af3696bc15d0ffcf89de984e
ToppCelldroplet-Trachea-3m-Mesenchymal-fibroblast-fibroblast_of_trachea-tracheal_fibroblast_l1|3m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

DUSP29 TNN CNTNAP2 CRISPLD1 BMP15

3.68e-061865654e983de6d2515082f9e555f4f949cec84281c140
ToppCellControl-Endothelial-VE_Capillary_A|Endothelial / Disease state, Lineage and Cell class

NEDD4L GVINP1 CHST2 ACE BTNL9

3.88e-0618856588b3415e33db81726dd29c1f50c886e057af50a0
ToppCellprimary_visual_cortex-Neuronal-GABAergic_neuron-Lamp5-Lamp5_Plch2_Dock5|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype

TGFB2 CNTNAP2 NOS1 CRISPLD1

4.01e-05152564fed80b467ec9e30c7f98bed6cc4f8c583b715e9e
ToppCellprimary_visual_cortex-Neuronal-GABAergic_neuron-Lamp5|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype

TGFB2 CNTNAP2 NOS1 CRISPLD1

5.27e-051635648d17f44faf0549fe71a9a45f811f50d767275414
ToppCell367C-Endothelial_cells-Endothelial-C_(Capillary_Aerocyte_)-|Endothelial_cells / Donor, Lineage, Cell class and subclass (all cells)

TNN CHST2 ACE BTNL9

6.06e-05169564225aec04ba762d4c55885257de03a65b63503fbb
ToppCell367C-Endothelial_cells-Endothelial-C_(Capillary_Aerocyte_)|Endothelial_cells / Donor, Lineage, Cell class and subclass (all cells)

TNN CHST2 ACE BTNL9

6.06e-05169564278960f940b646a788360b1c84d641a8d169896b
ToppCellP07-Mesenchymal-mesenchymal_fibroblast-mesothelial_cell_of_visceral_pleura|P07 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase

SULF2 PTCHD3 CNTNAP2 CPZ

6.49e-051725649a256db817c1af1802203cc88a55d608fb328c63
ToppCellfacs-Marrow-B-cells-24m|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CNTNAP2 CTSH NOS1 GALNT13

6.94e-05175564887e75fc90e59a6394d62f3c048a9cfdf6707725
ToppCellE18.5-Endothelial-Endothelial_blood-vessel-Macrovascular_EC-AEC-AEC_mature|E18.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

ACE BTNL9 CRISPLD1 BMP15

7.09e-0517656427e6b3ae41068d6cfdda3d46da7df2a27567140e
ToppCellE18.5-Endothelial-Endothelial_blood-vessel-Macrovascular_EC-AEC|E18.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

ACE BTNL9 CRISPLD1 BMP15

7.09e-05176564d6a5470af9592f34a741265f2ea9651c05c3add3
ToppCell368C-Lymphocytic-CD4_T-cell-Proliferating_T_cell|CD4_T-cell / Donor, Lineage, Cell class and subclass (all cells)

OPN1MW3 CNTNAP2 OPN1LW LARGE1

7.25e-05177564844017225e9039d1bc621a9630a30c2e9a51b36d
ToppCellTCGA-Colorectal-Primary_Tumor-Colorectal_Adenocarcinoma-Rectal_Adenocarcinoma-7|TCGA-Colorectal / Sample_Type by Project: Shred V9

TGFB2 PHF20 KDM2A CRISPLD1

7.41e-05178564edc76b8f15056ec1c9a1c61a048b6331a92592d6
ToppCellfacs-SCAT|facs / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BMP1 CPZ ACE CRISPLD1

7.74e-051805646c70b6b7480507fa94625013222ad338ee7dd1d9
ToppCellChildren_(3_yrs)-Epithelial-alveolar_epithelial_cell_type_2-D046|Children_(3_yrs) / Lineage, Cell type, age group and donor

BMP1 NEDD4L CTSH LARGE1

8.25e-051835646847c1252d6bb105524f812658112517fd351eab
ToppCell(4)_B_cells-(4)_B_mantle|(4)_B_cells / Spleen cell shreds - cell class (v1) and cell subclass (v1)

CNTNAP2 TSPO NSD3 LARGE1

8.25e-0518356421b7fb6482eb1d5d31a4029e47e0992e8ddc8e2c
ToppCellPBMC-Convalescent-Lymphocyte-B-B_cell-B_memory-B_memory-3|Convalescent / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

TNN CNTNAP2 CTSH BTNL9

8.60e-0518556405e6eb78ead81268c1656e7ffe34f9cb7329b908
ToppCellE17.5-Epithelial|E17.5 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase

TGFB2 TINAG NEDD4L CTSH

8.96e-05187564fdabe716ce67f2eede90548198cbe20bbf693570
ToppCellE17.5-Epithelial-epithelial_progenitor_cell-epithelial_progenitor_cell|E17.5 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase

TGFB2 TINAG NEDD4L CTSH

9.53e-051905648e9ba1f1af520564a1a7dfa9ef74ef5f0d0bf0d5
ToppCell3'_v3-Lung-Myeloid_Dendritic-DC2|Lung / Manually curated celltypes from each tissue

TGFB2 SULF2 CTSH PPP1R16A

9.53e-05190564468525c05e38158a3b8a445882b2d63dfb1d2c63
ToppCellChildren_(3_yrs)-Epithelial-alveolar_epithelial_cell_type_2|Children_(3_yrs) / Lineage, Cell type, age group and donor

BMP1 NEDD4L CTSH LARGE1

9.73e-05191564a0332a4ef629510fb313ec119195c44a3f704a80
ToppCellCOVID-19-Myeloid-DC2|COVID-19 / Condition, Lineage and Cell class

SULF2 CHST2 CTSH PPP1R16A

9.73e-051915641304ab7b5713f29f3966ffc020ea1b52e8e2f375
ToppCellE17.5-Epithelial-epithelial_progenitor_cell|E17.5 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase

TGFB2 TINAG NEDD4L CTSH

9.73e-0519156468b717fce7d9349ef56255ee0c5e57fc67e50fd8
ToppCellE15.5-Epithelial-epithelial_progenitor_cell-epithelial_progenitor_cell|E15.5 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase

TGFB2 BMP1 TINAG CTSH

9.73e-051915646f5d91a9583bbb30dfaa30dd9c7772995a9196be
ToppCellChildren_(3_yrs)-Epithelial|Children_(3_yrs) / Lineage, Cell type, age group and donor

BMP1 NEDD4L B4GALNT3 LARGE1

9.73e-05191564e432c6e1ae82dddf84314ce73d2b7a991630d905
ToppCellE15.5-Epithelial-epithelial_progenitor_cell|E15.5 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase

TGFB2 BMP1 TINAG CTSH

9.92e-05192564cb6f42dcffe650f7958543531d8f5412b2f2eb12
ToppCellEpithelial-alveolar_epithelial_cell_type_2|World / Lineage, Cell type, age group and donor

BMP1 NEDD4L CTSH LARGE1

9.92e-0519256458c3737be7acce39fd2b91d70d6d7b2bbaa4f710
ToppCell367C-Endothelial_cells-Endothelial-E-|Endothelial_cells / Donor, Lineage, Cell class and subclass (all cells)

TGFB2 NEDD4L ACE BTNL9

1.01e-041935645c6b03d6d98aa873fda1a201d44a912246bb5a92
ToppCellE18.5-Epithelial-Epithelial_Alveolar-Epithelial_Alveolar-AT1/AT2|E18.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

TGFB2 TINAG NEDD4L CTSH

1.01e-0419356454506c0da2f219f472b95e8935a78b657a8dec41
ToppCellnucseq-Epithelial-Epithelial_Alveolar-AT2-AT2|nucseq / Celltype signatures by Technology, Lineage, Lineage_subclass, Celltype_group, Cell_type2

BMP1 NEDD4L CTSH LARGE1

1.01e-04193564fd4d3c0d7caf8a2fff5b3d901fc28d19a8163cdf
ToppCellE16.5-Epithelial-Epithelial_Alveolar-Epithelial_Alveolar-Sox9_Epi-Sox9_Epi_mature|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

TGFB2 TINAG NEDD4L CTSH

1.01e-0419356433c495a2a7252b48ce10321642fd675d03cc80fc
ToppCellE18.5-Epithelial-Epithelial_Alveolar-Epithelial_Alveolar-AT1/AT2-AT1/AT2_mature|E18.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

TGFB2 TINAG NEDD4L CTSH

1.01e-041935642d42721fac1bee294ede47d609bebb3e7d36bf0c
ToppCell367C-Endothelial_cells-Endothelial-E|Endothelial_cells / Donor, Lineage, Cell class and subclass (all cells)

TGFB2 NEDD4L ACE BTNL9

1.01e-04193564d4b58eee97043b4337ec36c40f9af6499d864df9
ToppCellnucseq-Epithelial-Epithelial_Alveolar-AT2|nucseq / Celltype signatures by Technology, Lineage, Lineage_subclass, Celltype_group, Cell_type2

BMP1 NEDD4L CTSH LARGE1

1.01e-04193564f3cc7cfdbc164a4ed42f87647111522b7d393bcb
ToppCellIPF-Endothelial-VE_Capillary_A|Endothelial / Disease state, Lineage and Cell class

NEDD4L GVINP1 ACE BTNL9

1.03e-04194564777ce41c3f22c591e2d81120f189b834e53ffb4b
ToppCellChildren_(3_yrs)-Epithelial-alveolar_epithelial_cell_type_2-D032|Children_(3_yrs) / Lineage, Cell type, age group and donor

BMP1 NEDD4L CTSH LARGE1

1.03e-0419456497534c8bba895a7913665e03ae4e5c4a6ad71daf
ToppCellE16.5-Epithelial-Epithelial_Alveolar|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

TGFB2 TINAG NEDD4L CTSH

1.07e-041965641756254a61ea92601ed5e223ef4471f010c12216
ToppCellE16.5-Epithelial-Epithelial_Alveolar-Epithelial_Alveolar|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

TGFB2 TINAG NEDD4L CTSH

1.07e-04196564caa3c9555e1c656e88246ed31388a818f77610a1
ToppCell(1)_Osterolineage_cells-(11)_OLC-2|(1)_Osterolineage_cells / Cell class and subclass of bone marrow stroma cells in homeostatis

TGFB2 TNN TSPO CRISPLD1

1.12e-041985649f9dcf23ffb333105263132d87b90095642294cf
ToppCellParenchymal-10x5prime-Endothelial-Endothelia_vascular-VE_pulmonary_arterial|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations

SULF2 ACE BTNL9 NOS1

1.16e-04200564ac6b8bc9998d303f788511b8f111e682ea9f3df8
ToppCellSmart-start-Cell-Wel_seq-Non-neoplastic-Glial-Neuronal-OPC-OPC-F|Smart-start-Cell-Wel_seq / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

SULF2 CNTNAP2 NOS1 GALNT13

1.16e-04200564ad777683adeb2ce45ade570386235e311fa7ea2d
ToppCellThalamus-Endothelial-ENDOTHELIAL_STALK-Flt1_1-Endothelial_Stalk.Flt1.Car4_(Car4)-|Thalamus / BrainAtlas - Mouse McCarroll V32

GVINP1 CTSW BMP15

1.45e-0481563f7f2adf1fecd34b444de92d4c1bf45eb0281f4ad
ToppCellThalamus-Endothelial-ENDOTHELIAL_STALK-Flt1_1-Endothelial_Stalk.Flt1.Car4_(Car4)|Thalamus / BrainAtlas - Mouse McCarroll V32

GVINP1 CTSW BMP15

1.45e-04815638d323402ee5fb450947b00b0d75ca8f07aa4769e
ToppCellThalamus-Endothelial-ENDOTHELIAL_STALK-Flt1_1-Endothelial_Stalk.Flt1.Car4_(Car4)--|Thalamus / BrainAtlas - Mouse McCarroll V32

GVINP1 CTSW BMP15

1.45e-048156355cbf579d93e14bc4aebbed0fd11076c9313cdac
Drug4-methylumbelliferone

SUMF2 SULF2 AGL NAGLU MFSD8 CHST2

7.78e-07132556CID003364573
Diseaseblue cone monochromacy (implicated_via_orthology)

OPN1MW2 OPN1MW3 OPN1LW OPN1MW

1.08e-114554DOID:0050679 (implicated_via_orthology)
DiseaseMUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K

POMT2 B4GAT1 LARGE1

2.20e-0614553C1836373
Diseasealpha-Dystroglycanopathies

POMT2 B4GAT1 LARGE1

2.20e-0614553C2936406
DiseaseMuscle eye brain disease

POMT2 B4GAT1 LARGE1

2.20e-0614553C0457133
DiseaseFukuyama Type Congenital Muscular Dystrophy

POMT2 B4GAT1 LARGE1

2.20e-0614553C0410174
DiseaseMuscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1

POMT2 B4GAT1 LARGE1

2.20e-0614553C4284790
DiseaseWalker-Warburg congenital muscular dystrophy

POMT2 B4GAT1 LARGE1

2.74e-0615553C0265221
DiseaseCone monochromatism

OPN1LW OPN1MW

3.41e-062552C0339537
DiseaseBLUE CONE MONOCHROMACY

OPN1LW OPN1MW

3.41e-062552303700
DiseaseCone monochromatism

OPN1LW OPN1MW

3.41e-062552cv:C0339537
Diseaseblue cone monochromacy (is_implicated_in)

OPN1LW OPN1MW

3.41e-062552DOID:0050679 (is_implicated_in)
DiseaseBORNHOLM EYE DISEASE

OPN1LW OPN1MW

3.41e-062552C3159311
DiseaseAchromatopsia incomplete, X-linked

OPN1LW OPN1MW

3.41e-062552C2931753
DiseaseRed-green dyschromatopsia

OPN1LW OPN1MW

3.41e-062552cv:C0155016
DiseaseChronic Liver Failure

TSPO NOS1

2.04e-054552C2936476
Diseaseamino acid metabolic disorder (implicated_via_orthology)

TARS3 TARS1

2.04e-054552DOID:9252 (implicated_via_orthology)
DiseaseEnd Stage Liver Disease

TSPO NOS1

2.04e-054552C0745744
DiseaseMuscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1

POMT2 LARGE1

3.40e-055552cv:C4284790
DiseaseMUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1

POMT2 LARGE1

3.40e-055552236670
DiseaseQualitative or quantitative defects of alpha-dystroglycan

POMT2 LARGE1

5.09e-056552cv:C2936406
DiseaseWalker-Warburg syndrome (implicated_via_orthology)

POMT2 B4GAT1

7.12e-057552DOID:0050560 (implicated_via_orthology)
Diseasemuscular dystrophy-dystroglycanopathy type B1 (implicated_via_orthology)

B4GAT1 LARGE1

9.48e-058552DOID:0050588 (implicated_via_orthology)
DiseaseCongenital muscular dystrophy

POMT2 LARGE1

2.22e-0412552cv:C0699743
DiseaseHepatic Encephalopathy

TSPO NOS1

2.63e-0413552C0019151
DiseaseHepatic Coma

TSPO NOS1

2.63e-0413552C0019147
DiseaseFulminant Hepatic Failure with Cerebral Edema

TSPO NOS1

2.63e-0413552C0751197
DiseaseHepatic Stupor

TSPO NOS1

2.63e-0413552C0751198
Diseaseglycerol-3-phosphate measurement

NEDD4L CNTNAP2

3.53e-0415552EFO_0010488
Diseasebody fat distribution

TGFB2 KDM2A CPZ B4GALNT3

5.53e-04202554EFO_0004341
Diseaserenovascular hypertension (biomarker_via_orthology)

ACE NOS1

5.72e-0419552DOID:1591 (biomarker_via_orthology)
Diseaseend stage renal disease (implicated_via_orthology)

ACE NOS1

6.34e-0420552DOID:783 (implicated_via_orthology)
Diseasedepressive disorder (implicated_via_orthology)

DRD5 NOS1

7.69e-0422552DOID:1596 (implicated_via_orthology)
DiseaseAttention deficit hyperactivity disorder

DRD5 MED13

9.17e-0424552C1263846
DiseaseDepressive Symptoms

TXNRD2 ACE

1.08e-0326552C0086132
DiseaseCone-Rod Dystrophy 2

OPN1LW OPN1MW

1.34e-0329552C3489532
DiseaseUnipolar Depression

DRD5 CNTNAP2 ACE NOS1

1.39e-03259554C0041696

Protein segments in the cluster

PeptideGeneStartEntry
SPHLKYWVPFIWFGN

BEST3

176

Q8N1M1
SGWYPKPKVQWRDHQ

BTNL9

176

Q6UXG8
QNGEVLGWPEYQWHP

ACE

616

P12821
GEKLGWPQYNWTPNS

ACE

1216

P12821
WQDPWEPFYVAGGKV

B4GAT1

321

O43505
PQWPEGYWEVNGFGL

B4GALNT3

916

Q6L9W6
VNQGPLHLGGIYWWK

GVINP1

351

Q7Z2Y8
GWPKEYPPNKNCIWQ

BMP1

606

P13497
GWLFQHQPQFWGPAQ

NAGLU

351

P54802
PPIFGWSRYWPHGLK

OPN1LW

186

P04000
PPIFGWSRYWPHGLK

OPN1MW3

186

P0DN78
PWKAVAEVAGYWPFG

DRD5

96

P21918
PWGNQFPKIQWEDLH

MFSD8

356

Q8NHS3
PPIFGWSRYWPHGLK

OPN1MW2

186

P0DN77
DFWIRWYQQKPGNPP

IGLV5-52

51

A0A0A0MRZ9
PFNPWNWGKLAEAYL

C8orf76

161

Q96K31
WYLGNLWKNHRPWPA

LARGE1

276

O95461
GPGDVLYIPMYWWHH

HIF1AN

266

Q9NWT6
RQLGWDHWIIAPPFY

BMP15

301

O95972
KPNGQAIAWYTPIHW

LMNTD1

241

Q8N9Z9
LHWGEPKTWYGVPGY

KDM5B

511

Q9UGL1
YQPDPWNTHVWKGTN

NOS1

711

P29475
PPIFGWSRYWPHGLK

OPN1MW

186

P04001
GGFNWKLNFRWYPVP

GALNT13

256

Q8IUC8
LYWHKHGDGWKTPVP

MLXIP

251

Q9HAP2
FWKRPPQRWSGQEHY

CCSER2

591

Q9H7U1
WYHIHQGGKVFWLIP

KDM2A

221

Q9Y2K7
IPIPQHYWWGKVAPE

CPZ

346

Q66K79
WKGSPQYTHVNEVWP

DUSP29

46

Q68J44
YSPKGNWWGHAPYKH

CRISPLD1

206

Q9H336
NWWGHAPYKHGRPCS

CRISPLD1

211

Q9H336
FPQPPKQNWFWGHQG

CYP4F11

51

Q9HBI6
PHPTPYWILKNSWGA

CTSW

321

P56202
AFGPVAQPYLWWKKH

ELOVL1

186

Q9BW60
KNGIPYWIVKNSWGP

CTSH

291

P09668
FHAGWEQPHWFYKPG

DMGDH

486

Q9UI17
GPAGWHRFWYQVVIP

DND1

281

Q8IYX4
GRNWKPYHQDGNIWA

CNTNAP2

121

Q9UHC6
GWQVGAHPWIFLLAP

PTCHD3

131

Q3KNS1
PGQRPGFKYWYDKEW

PHF20

701

Q9BVI0
NYGGKWPFWLSPRQV

TARS3

686

A2RTX5
ENYGGKWPFWLSPRQ

TARS1

606

P26639
PWWEQQGFFKPEYGR

VARS1

311

P26640
GLKGQVYPWGNWFQP

SUMF2

176

Q8NBJ7
KPWHWPINYQGLRFS

POMT2

566

Q9UKY4
WEPLHAAAYWGQVPL

PPP1R16A

266

Q96I34
PWGVQGPLTWQQFHK

MED13

1301

Q9UHV7
PVWHVWQKLYPGDAV

CHST2

196

Q9Y4C5
GWKWIHEPKGYNANF

TGFB2

331

P61812
NWEPWKGHEFSIPYV

TNN

1256

Q9UQP3
GSKNWIRPCPWNYGQ

TGM5

171

O43548
NLTQPPYGKWECPWH

NSD3

1351

Q9BZ95
PNYGWEVAQPVPHDW

TXNRD2

111

Q9NNW7
GWDGKPIPYWLYKLH

SF3A3

386

Q12874
FVASYKWPGWTHGPL

TINAG

221

Q9UJW2
NEYNGSYVPPGWKEW

SULF2

146

Q8IWU5
LRWYAGLQKPSWHPP

TSPO

31

P30536
KGFNYHQGPEWLWPI

AGL

1441

P35573
HQGPEWLWPIGYFLR

AGL

1446

P35573
NGYCPNHPVIQWFWK

NEDD4L

871

Q96PU5