decreased central vision Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007663
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Genes

12 genes associated with the decreased central vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
BEST1 bestrophin 1
CLRN1 clarin 1
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
PDE6H phosphodiesterase 6H, cGMP-specific, cone, gamma
PITPNM3 PITPNM family member 3
PROM1 prominin 1
RPE65 retinal pigment epithelium-specific protein 65kDa
RPGR retinitis pigmentosa GTPase regulator
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
TRPM1 transient receptor potential cation channel, subfamily M, member 1