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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:9008296
Term: Eye Abnormalities
Definition: Congenital absence of or defects in structures of the eye; may also be hereditary.
Definition Source(s): MESH:D005124
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: Abnormality of the eyePMID:28041643 PMID:28492532 PMID:28795510 PMID:29053603
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Abnormality of the eyePMID:28041643 PMID:28492532 PMID:28795510
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Abnormality of the eyePMID:10888875 PMID:10958649 PMID:12815043 PMID:1347967 PMID:14757870 PMID:15161866 PMID:15657609 PMID:15712225 PMID:16379026 PMID:17265047 PMID:19592100 PMID:23805033 PMID:24033266 PMID:25741868 PMID:25770143 PMID:28041643 PMID:28492532 PMID:28795510 PMID:30544257 PMID:30718709 PMID:32860008 PMID:33546218 PMID:36909829
CNGB3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Abnormality of the eyePMID:15161866 PMID:16379026 PMID:22975760 PMID:22995991 PMID:24504161 PMID:25741868 PMID:28418496 PMID:28492532 PMID:28795510 PMID:30418171 PMID:32869108
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