DRD2

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is agene
is mentioned by
Full namedopamine receptor D2
EntrezGene1813
PheGenI1813
VariationViewer1813
dbSNP1813
SADR1813
HugeNav1813
wikipediaDRD2
googleDRD2
gopubmedDRD2
EVSDRD2
HEFalMpDRD2
23andMeDRD2
UniProtP14416
EnsemblENSG00000149295
OMIM126450
EVSDRD2
# SNPs32
  Max Magnitude Chromosome position Summary
Rs104894220 0 113,287,657
Rs1076560 2 113,283,688
Rs1076562 113,296,008
Rs1079596 113,296,619
Rs1079597 113,296,286
Rs1079598 113,296,274
Rs1079727 113,289,182
Rs11214606 0 113,309,869
Rs11214613 0 113,335,259
Rs1124493 113,282,295
Rs1125394 113,297,185
Rs12363125 113,285,916
Rs12364283 0 113,346,955
Rs1554929 113,278,764
Rs1799732 2 113,346,251
Rs1799978 0 113,346,351
Rs1800496 0 113,283,488
Rs1800498 113,291,588
Rs1801028 0 113,283,484
Rs2234689 113,278,483
Rs2242592 113,279,430
Rs2283265 113,285,536
Rs2734839 113,286,490
Rs2734841 113,281,776
Rs2734842 113,280,274
Rs4436578 113,306,765
Rs4648317 1.2 113,331,532
Rs4648319 113,314,363
Rs6275 113,283,477
Rs6276 113,281,397
Rs6277 2 113,283,459
Rs6279 113,281,073

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.