attenuation of retinal blood vessels Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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21 genes associated with the attenuation of retinal blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
BEST1 bestrophin 1
C2ORF71 chromosome 2 open reading frame 71
CERKL ceramide kinase-like
CLRN1 clarin 1
EYS eyes shut homolog (Drosophila)
FSCN2 fascin actin-bundling protein 2, retinal
IDH3B isocitrate dehydrogenase 3 (NAD+) beta
NMNAT1 nicotinamide nucleotide adenylyltransferase 1
PDE6A phosphodiesterase 6A, cGMP-specific, rod, alpha
PDE6G phosphodiesterase 6G, cGMP-specific, rod, gamma
PRCD progressive rod-cone degeneration
RGR retinal G protein coupled receptor
RPE65 retinal pigment epithelium-specific protein 65kDa
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
SNRNP200 small nuclear ribonucleoprotein 200kDa (U5)
TOPORS topoisomerase I binding, arginine/serine-rich, E3 ubiquitin protein ligase
TTC8 tetratricopeptide repeat domain 8
USH2A Usher syndrome 2A (autosomal recessive, mild)
ZNF513 zinc finger protein 513