decreased electroretinogram (erg) amplitude Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Descreased amplitude of eletrical response upon electroretinography. (Human Phenotype Ontology, HP_0000654)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000654
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Genes

14 genes associated with the decreased electroretinogram (erg) amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACOX1 acyl-CoA oxidase 1, palmitoyl
ALG3 ALG3, alpha-1,3- mannosyltransferase
BEST1 bestrophin 1
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
IDH3B isocitrate dehydrogenase 3 (NAD+) beta
LARGE like-glycosyltransferase
LRAT lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
MCOLN1 mucolipin 1
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
PPT1 palmitoyl-protein thioesterase 1
RGR retinal G protein coupled receptor
RHO rhodopsin
RPE65 retinal pigment epithelium-specific protein 65kDa
SAG S-antigen; retina and pineal gland (arrestin)