constricted visual fields Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001133
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Genes

18 genes associated with the constricted visual fields phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CERKL ceramide kinase-like
CHM choroideremia (Rab escort protein 1)
CYP4V2 cytochrome P450, family 4, subfamily V, polypeptide 2
EYS eyes shut homolog (Drosophila)
FAM161A family with sequence similarity 161, member A
IDH3B isocitrate dehydrogenase 3 (NAD+) beta
IMPDH1 IMP (inosine 5'-monophosphate) dehydrogenase 1
PRPF8 pre-mRNA processing factor 8
RBP3 retinol binding protein 3, interstitial
RGR retinal G protein coupled receptor
RP1 retinitis pigmentosa 1 (autosomal dominant)
RP2 retinitis pigmentosa 2 (X-linked recessive)
RP9 retinitis pigmentosa 9 (autosomal dominant)
SH3BP2 SH3-domain binding protein 2
SOST sclerostin
SPATA7 spermatogenesis associated 7
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast)
TMEM126A transmembrane protein 126A