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GENE - TERM ANNOTATION REPORT

RGD ID: 8719421
Species: Chinchilla lanigera
RGD Object: Gene
Symbol: Slc2a1
Name: solute carrier family 2 member 1
Acc ID: DOID:10907
Term: microcephaly
Definition: A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/Microcephaly "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)
Slc2a1 ISOSLC2A1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: MicrocephalyPMID:10980529 PMID:20129935 PMID:21832227 PMID:25326635 PMID:25741868 PMID:26193382 PMID:26216499 PMID:28492532 PMID:32581362
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