Fundus Albipunctatus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A fundus dystrophy that is characterized by discrete uniform white dots over the entire fundus with greatest density in the midperiphery and no macular involvement. (Human Disease Ontology, DOID_11105)
External Link https://www.disgenet.org/browser/0/1/0/C0311338
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Genes

9 genes associated with the disease Fundus Albipunctatus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ERG v-ets avian erythroblastosis virus E26 oncogene homolog
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1
MFRP membrane frizzled-related protein
PRPH2 peripherin 2 (retinal degeneration, slow)
RDH12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
RDH5 retinol dehydrogenase 5 (11-cis/9-cis)
RHO rhodopsin
RLBP1 retinaldehyde binding protein 1
RPE65 retinal pigment epithelium-specific protein 65kDa