choroidal sclerosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_980)
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20 genes co-occuring with the disease choroidal sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PRPH2 peripherin 2 (retinal degeneration, slow) 1.89314
GUCA1A guanylate cyclase activator 1A (retina) 1.70087
GUCY2D guanylate cyclase 2D, membrane (retina-specific) 1.67683
PITPNA phosphatidylinositol transfer protein, alpha 1.56489
CYP4V2 cytochrome P450, family 4, subfamily V, polypeptide 2 1.3494
UNC119 unc-119 homolog (C. elegans) 1.29702
RIMS1 regulating synaptic membrane exocytosis 1 1.24558
TIMP3 TIMP metallopeptidase inhibitor 3 1.13332
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 1.01976
RING1 ring finger protein 1 1.01891
AIPL1 aryl hydrocarbon receptor interacting protein-like 1 0.977585
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1 0.926692
ERG v-ets avian erythroblastosis virus E26 oncogene homolog 0.918848
ARRB2 arrestin, beta 2 0.864684
RCVRN recoverin 0.829049
PLIN2 perilipin 2 0.760231
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa) 0.760231
NPR1 natriuretic peptide receptor 1 0.469576
GUCY2C guanylate cyclase 2C 0.468441
PROM1 prominin 1 0.292616