DRD2 Chromosome 11

Dopamine receptor D2
4 variants 4 Health Risk

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What This Gene Does
This gene encodes the D2 subtype of the dopamine receptor. This G-protein coupled receptor inhibits adenylyl cyclase activity. A missense mutation in this gene causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing of this gene results in two transcript variants encoding different isoforms. A third variant has been described, but it has not been determined whether this form is normal or due to aberrant splicing. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Dopamine receptors|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
11q23.2
Ensembl
ENSG00000149295
Associated Conditions (2)
Dystonic disorder
DRD2-associated Dystonia
Key Variants
All Variants (4)
RSID Category Clinical Significance Conditions
RS138873192 Health Risk Conflicting classifications of pathogenicity Dystonic disorder, Dystonic disorder
RS1800496 Health Risk Conflicting classifications of pathogenicity Dystonic disorder, DRD2-associated Dystonia, Dystonic disorder
RS201137518 Health Risk Conflicting classifications of pathogenicity Dystonic disorder, Dystonic disorder
RS747312255 Health Risk Conflicting classifications of pathogenicity Dystonic disorder, Dystonic disorder
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