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GENE - TERM ANNOTATION REPORT

RGD ID: 1560033
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Gpr179
Name: G protein-coupled receptor 179
Acc ID: DOID:0050534
Term: congenital stationary night blindness
Definition: A hereditary night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves. (DO)
Definition Source(s): http://disorders.eyes.arizona.edu/disorders/night-blindness-congenital-stationary-csnbad3 "DO" "DO", http://www.ncbi.nlm.nih.gov/books/NBK1245/ "DO" "DO", http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1772254/ "DO" "DO", http://www.omim.org/entry/610444 "DO" "DO", http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=215 "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Gpr179 ISOGPR179 (Homo sapiens)11554173CTDCTD Direct Evidence: marker/mechanism 
Gpr179 ISOGPR179 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital Stationary Night Blindness, Recessive | ClinVar Annotator: match by term: Congenital stationary night blindnessPMID:22325361 PMID:22325362 PMID:24033266 PMID:25741868 PMID:28041643 PMID:28492532 PMID:30487145 PMID:30609409 PMID:31589614 PMID:31964843 PMID:31980526 PMID:32531858 PMID:32581362 PMID:36460718
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