absent rod-and cone-mediated responses on erg Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the combined rod-and-code response on electroretinogram. (Human Phenotype Ontology, HP_0007688)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007688
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Genes

8 genes associated with the absent rod-and cone-mediated responses on erg phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
CERKL ceramide kinase-like
CLRN1 clarin 1
IMPDH1 IMP (inosine 5'-monophosphate) dehydrogenase 1
NR2E3 nuclear receptor subfamily 2, group E, member 3
RP1 retinitis pigmentosa 1 (autosomal dominant)
RP9 retinitis pigmentosa 9 (autosomal dominant)
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1