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DRD2 gene

dopamine receptor D2

Key facts

Official symbol
DRD2
Full name
DRD2
Chromosome
11
Map location
11q23.2
Organism
Homo sapiens
NCBI Gene ID
1813
Also known as
D2DR, D2R

Function summary

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].

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Data source: NCBI Gene · alsesAI Gene Library