" /> DRD2 2 Allele - CISMeF





Preferred Label : DRD2 2 Allele;

NCIt synonyms : DRD2 A2 Allele; Dopamine Receptor D2 A2 Allele; DRD2-A2 Allele; TaqI A2 Allele;

NCIt definition : Human DRD2 Gene at 11q23 encodes Dopamine Receptor D2, a G-protein coupled receptor that inhibits adenylyl cyclase activity. Missense mutation in DRD2 causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing results in two different isoforms. A third variant has been described, but it has not been determined whether this form is normal or due to aberrant splicing. Different alleles are associated with increased incidence of substance abuse. (NCI);

GenBank Accession Number : NM_000795;

Details


Keyword's position in hierarchy(ies) : arborescence

You can consult :


Nous contacter.
08/07/2025


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.