fundus albipunctatus Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
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)
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Genes

23 genes co-occuring with the disease fundus albipunctatus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
RDH5 retinol dehydrogenase 5 (11-cis/9-cis) 3.52197
SDR9C7 short chain dehydrogenase/reductase family 9C, member 7 1.86873
RLBP1 retinaldehyde binding protein 1 1.7555
RDH12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis) 1.54274
RHD Rh blood group, D antigen 1.45089
RDH10 retinol dehydrogenase 10 (all-trans) 1.35899
GRK1 G protein-coupled receptor kinase 1 1.20613
RHO rhodopsin 1.1473
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit 1.14433
PLA2G5 phospholipase A2, group V 1.11772
LRAT lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase) 1.08579
GNAT1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1 1.03282
RDH8 retinol dehydrogenase 8 (all-trans) 1.02271
RPE65 retinal pigment epithelium-specific protein 65kDa 0.821257
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 0.783526
NYX nyctalopin 0.758601
RS1 retinoschisin 1 0.756156
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta 0.693098
ATXN7 ataxin 7 0.67312
RDH11 retinol dehydrogenase 11 (all-trans/9-cis/11-cis) 0.648138
BBS2 Bardet-Biedl syndrome 2 0.455601
RBP3 retinol binding protein 3, interstitial 0.415773
SAG S-antigen; retina and pineal gland (arrestin) 0.295851