Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		cyclic nucleotide gated channel subunit alpha 3 0.650 0.154 8.0E-20
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.430 None 1.000 0 0 2004 2018
Entrez Id: 54714
Gene Symbol: CNGB3
CNGB3 		cyclic nucleotide gated channel subunit beta 3 0.633 0.192 7.8E-19
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.420 None 1.000 0 0 2004 2018
Entrez Id: 2780
Gene Symbol: GNAT2
GNAT2 		G protein subunit alpha transducin 2 0.674 0.231 7.0E-06
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.410 None 1.000 0 0 2002 2002
Entrez Id: 22926
Gene Symbol: ATF6
ATF6 		activating transcription factor 6 0.516 0.846 3.2E-07
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.400 None 1.000 0 0 2015 2015
Entrez Id: 4976
Gene Symbol: OPA1
OPA1 		OPA1 mitochondrial dynamin like GTPase 0.510 0.846 0.99
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.110 None 1.000 0 0 2010 2010
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		synuclein alpha 0.427 0.885 0.88
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 6663
Gene Symbol: SOX10
SOX10 		SRY-box transcription factor 10 0.461 0.808 0.99
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 6785
Gene Symbol: ELOVL4
ELOVL4 		ELOVL fatty acid elongase 4 0.601 0.577 0.83
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 6870
Gene Symbol: TACR3
TACR3 		tachykinin receptor 3 0.553 0.769 1.8E-17
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 7287
Gene Symbol: TULP1
TULP1 		TUB like protein 1 0.623 0.462 5.7E-04
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 7345
Gene Symbol: UCHL1
UCHL1 		ubiquitin C-terminal hydrolase L1 0.482 0.885 0.99
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 65018
Gene Symbol: PINK1
PINK1 		PTEN induced kinase 1 0.516 0.769 1.9E-10
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 64802
Gene Symbol: NMNAT1
NMNAT1 		nicotinamide nucleotide adenylyltransferase 1 0.656 0.269 3.5E-02
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 55717
Gene Symbol: WDR11
WDR11 		WD repeat domain 11 0.524 0.808 1.4E-08
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 57096
Gene Symbol: RPGRIP1
RPGRIP1 		RPGR interacting protein 1 0.553 0.654 1.3E-23
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		peripherin 2 0.551 0.500 0.12
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 6017
Gene Symbol: RLBP1
RLBP1 		retinaldehyde binding protein 1 0.644 0.500 1.1E-05
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 60675
Gene Symbol: PROK2
PROK2 		prokineticin 2 0.555 0.769 1.4E-02
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 6103
Gene Symbol: RPGR
RPGR 		retinitis pigmentosa GTPase regulator 0.536 0.692 1.00
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 64218
Gene Symbol: SEMA4A
SEMA4A 		semaphorin 4A 0.569 0.692 1.8E-05
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 7439
Gene Symbol: BEST1
BEST1 		bestrophin 1 0.465 0.885 1.8E-12
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 755
Gene Symbol: CFAP410
CFAP410 		cilia and flagella associated protein 410 0.633 0.615 3.3E-07
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 8822
Gene Symbol: FGF17
FGF17 		fibroblast growth factor 17 0.593 0.692 0.96
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0
Entrez Id: 8842
Gene Symbol: PROM1
PROM1 		prominin 1 0.410 0.846 1.9E-22
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype 0.100 None 0 0