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DRD2

From SNPedia
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is agene
is mentioned by
Full namedopamine receptor D2
EntrezGene1813
PheGenI1813
VariationViewer1813
ClinVarDRD2
dbSNP1813
SADR1813
HugeNav1813
wikipediaDRD2
googleDRD2
gopubmedDRD2
EVSDRD2
HEFalMpDRD2
23andMeDRD2
UniProtP14416
EnsemblENSG00000149295
OMIM126450
EVSDRD2
# SNPs33
  Max Magnitude Chromosome position Summary
Rs104894220 0 113,416,935
Rs1076560 2 113,412,966
Rs1076562 113,425,286
Rs1079596 113,425,897
Rs1079597 113,425,564
Rs1079598 113,425,552
Rs1079727 113,418,460
Rs11214606 0 113,439,147
Rs11214613 0 113,464,537
Rs1124493 113,411,573
Rs1125394 113,426,463
Rs12363125 113,415,194
Rs12364283 0 113,476,233
Rs1554929 113,408,042
Rs1799732 2 113,475,529
Rs1799978 0 113,475,629
Rs1800496 0 113,412,766
Rs1800498 113,420,866
Rs1801028 0 113,412,762
Rs2234689 113,407,761
Rs2242592 113,408,708
Rs2283265 113,414,814
Rs2734839 113,415,768
Rs2734841 113,411,054
Rs2734842 113,409,552
Rs4436578 113,436,043
Rs4648317 1.2 113,460,810
Rs4648319 113,443,641
Rs4938019 113,470,669
Rs6275 113,412,755
Rs6276 113,410,675
Rs6277 2 113,412,737
Rs6279 113,410,351

SNPs in DRD2 include:

[PMID 18063800] Genetically determined differences in learning from errors.

[1] Compared with DRD2 A1 carriers, subjects homozygous for the DRD2 A2 allele performed poorer in a measure of general cognitive functioning (MMSE) and in long term verbal memory. Our findings suggest that among the aged with cognitive impairments, the homozygous status for the A2 allele of the DRD2 Taq I polymorphism is associated with diminished cognitive performance and increased atrophy in the striatum.