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GENE - TERM ANNOTATION REPORT

RGD ID: 13920827
Species: Sus scrofa
RGD Object: Gene
Symbol: DRD2
Name: dopamine receptor D2
Acc ID: DOID:480
Term: movement disease
Definition: A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/Movement_disorders "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)
DRD2 ISODRD2 (Homo sapiens)9068941RGDmyoclonus dystonia, OMIM:159900, V154IPMID:10220438 REF_RGD_ID:1600903
DRD2 ISODRD2 (Homo sapiens)9068941CTDCTD Direct Evidence: marker/mechanismPMID:6858777
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