CYGB, cytoglobin, 114757

N. diseases: 88; N. variants: 6
Disease: RETINITIS PIGMENTOSA 36 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918369
rs121918369
Entrez Id: 114757;768206
Gene Symbol: CYGB;PRCD
CYGB;PRCD
CUI: C1864621
Disease:
RETINITIS PIGMENTOSA 36 		0.800 GeneticVariation UNIPROT Palmitoylation of Progressive Rod-Cone Degeneration (PRCD) Regulates Protein Stability and Localization. 27613864 2016
dbSNP: rs121918369
rs121918369
Entrez Id: 114757;768206
Gene Symbol: CYGB;PRCD
CYGB;PRCD
CUI: C1864621
Disease:
RETINITIS PIGMENTOSA 36 		0.800 GeneticVariation UNIPROT The progressive rod-cone degeneration (PRCD) protein is secreted through the conventional ER/Golgi-dependent pathway. 24992209 2014
dbSNP: rs121918369
rs121918369
Entrez Id: 114757;768206
Gene Symbol: CYGB;PRCD
CYGB;PRCD
CUI: C1864621
Disease:
RETINITIS PIGMENTOSA 36 		0.800 GeneticVariation UNIPROT Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans. 16938425 2006
dbSNP: rs121918369
rs121918369
Entrez Id: 114757;768206
Gene Symbol: CYGB;PRCD
CYGB;PRCD
CUI: C1864621
Disease:
RETINITIS PIGMENTOSA 36 		A 0.800 CausalMutation CLINVAR
dbSNP: rs387907268
rs387907268
Entrez Id: 114757;768206
Gene Symbol: CYGB;PRCD
CYGB;PRCD
CUI: C1864621
Disease:
RETINITIS PIGMENTOSA 36 		T 0.700 CausalMutation CLINVAR
dbSNP: rs767439982
rs767439982
Entrez Id: 114757;768206
Gene Symbol: CYGB;PRCD
CYGB;PRCD
CUI: C1864621
Disease:
RETINITIS PIGMENTOSA 36 		0.700 GeneticVariation UNIPROT