pigmentary retinal degeneration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001146
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Genes

10 genes associated with the pigmentary retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATXN7 ataxin 7
FZD4 frizzled class receptor 4
LRP5 low density lipoprotein receptor-related protein 5
MTTP microsomal triglyceride transfer protein
NR2E3 nuclear receptor subfamily 2, group E, member 3
PRPH2 peripherin 2 (retinal degeneration, slow)
ROM1 retinal outer segment membrane protein 1
SAG S-antigen; retina and pineal gland (arrestin)
TREX1 three prime repair exonuclease 1
TSPAN12 tetraspanin 12