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GENE - TERM ANNOTATION REPORT

RGD ID: 62259
Species: Mus musculus
RGD Object: Gene
Symbol: Gabrg2
Name: gamma-aminobutyric acid type A receptor, subunit gamma 2
Acc ID: DOID:0050561
Term: Lennox-Gastaut syndrome
Definition: A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood. (DO)
Definition Source(s): https://ghr.nlm.nih.gov/condition/lennox-gastaut-syndrome "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)
Gabrg2 ISOGABRG2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Lennox-Gastaut syndromePMID:22539854 PMID:22750526 PMID:24407264 PMID:25741868 PMID:27066572 PMID:28492532
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