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GENE - TERM ANNOTATION REPORT

RGD ID: 628608
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Slc16a2
Name: solute carrier family 16 member 2
Acc ID: DOID:630
Term: genetic disease
Definition: A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/ "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)
Slc16a2 ISOSLC16A2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:15980113 PMID:16974106 PMID:18398436 PMID:18414213 PMID:18636565 PMID:19194886 PMID:20301789 PMID:21835051 PMID:23568789 PMID:24265446 PMID:24721225 PMID:25527620 PMID:25741868 PMID:27212794 PMID:27805744 PMID:28492532
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