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: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		disease 0.970 strong 1.000 0 2 1993 2019
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C3887980
Disease: Protanomaly
Protanomaly 		disease 0.620 None 1.000 0 0 2002 2019
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		disease 0.110 None 1.000 0 1 2017 2017
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: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		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: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		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: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		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: C1845977
Disease: X- linked recessive
X- linked recessive 		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: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		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: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		disease 0.100 None 0 0
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		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: C0085636
Disease: Photophobia
Photophobia 		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: C0028738
Disease: Nystagmus
Nystagmus 		disease 0.100 None 0 0
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		disease 0.100 None 0 0
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C0027092
Disease: Myopia
Myopia 		disease 0.100 None 0 0
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C0010036
Disease: Corneal dystrophy
Corneal dystrophy 		disease 0.100 None 0 0
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW 		opsin 1, long wave sensitive 0.497 0.808 0.98
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0