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GENE - TERM ANNOTATION REPORT

RGD ID: 1352344
Species: Homo sapiens
RGD Object: Gene
Symbol: CNGB3
Name: cyclic nucleotide gated channel subunit beta 3
Acc ID: DOID:0050817
Term: Stargardt disease
Definition: An age related macular degeneration that is characterized by progressive vision loss usually to the point of legal blindness. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Stargardt_disease "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)
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:15712225 PMID:25741868 PMID:28492532
CNGB3 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:25741868 PMID:28492532
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:25741868 PMID:28492532 PMID:28795510
CNGB3 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGD 
CNGB3 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:28492532
CNGB3 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:25741868
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:15223812 PMID:28492532
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:15712225 PMID:28492532
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:15712225 PMID:25474149 PMID:26106334 PMID:28492532 PMID:28795510 PMID:31544997 PMID:32913385 PMID:35672425
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:15161866 PMID:16379026 PMID:22975760 PMID:22995991 PMID:24504161 PMID:25741868 PMID:28418496 PMID:28492532 PMID:28795510 PMID:30418171 PMID:32869108
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: STGDPMID:23776498 PMID:25741868 PMID:28492532
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