GPR179, G protein-coupled receptor 179, 440435

N. diseases: 23; N. variants: 13
Disease: Complete congenital stationary night blindness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4048798
Disease: Complete congenital stationary night blindness
Complete congenital stationary night blindness 		0.030 AlteredExpression disease BEFREE Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness. 24222301 2013
CUI: C4048798
Disease: Complete congenital stationary night blindness
Complete congenital stationary night blindness 		0.030 GeneticVariation disease BEFREE Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness. 22325361 2012
CUI: C4048798
Disease: Complete congenital stationary night blindness
Complete congenital stationary night blindness 		0.030 GeneticVariation disease BEFREE Candidate gene analysis of GPR179 in DNA extracted from patients with cCSNB identified GPR179-inactivating mutations in two patients. 22325362 2012