About: Rs1800955

An Entity of Type: Polymorphism111493266, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

In genetics, rs1800955 (also written as C-521T and -521C/T) is a single nucleotide polymorphism (SNP).It is located in the promoter region of the DRD4 gene.This gene codes for the dopamine receptor D4. Due to the dopamine hypothesis of schizophrenia the SNP has been investigated for link to schizophrenia, and it may be slightly associated with this disorder.

Property Value
dbo:abstract
  • In genetics, rs1800955 (also written as C-521T and -521C/T) is a single nucleotide polymorphism (SNP).It is located in the promoter region of the DRD4 gene.This gene codes for the dopamine receptor D4. Due to the dopamine hypothesis of schizophrenia the SNP has been investigated for link to schizophrenia, and it may be slightly associated with this disorder. The SNP has been investigated with respect to novelty seeking, — a personality trait that may be measured with the Temperament and Character Inventory.A 2008 meta-analysis indicates a possible association between novelty seeking and C-521T though rather small. (en)
dbo:wikiPageExternalLink
dbo:wikiPageID
  • 19189326 (xsd:integer)
dbo:wikiPageLength
  • 2915 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID
  • 1109062333 (xsd:integer)
dbo:wikiPageWikiLink
dbp:alfred
  • SI000215I (en)
dbp:chromosome
  • 11 (xsd:integer)
dbp:gene
  • DRD4 (en)
dbp:name
  • -521 (xsd:integer)
  • C-521T (en)
dbp:region
  • Promoter (en)
dbp:rsid
  • 1800955 (xsd:integer)
dbp:szgeneGeneid
  • 94 (xsd:integer)
dbp:szgenePolyid
  • 801 (xsd:integer)
dbp:wikiPageUsesTemplate
dcterms:subject
gold:hypernym
rdf:type
rdfs:comment
  • In genetics, rs1800955 (also written as C-521T and -521C/T) is a single nucleotide polymorphism (SNP).It is located in the promoter region of the DRD4 gene.This gene codes for the dopamine receptor D4. Due to the dopamine hypothesis of schizophrenia the SNP has been investigated for link to schizophrenia, and it may be slightly associated with this disorder. (en)
rdfs:label
  • Rs1800955 (en)
owl:sameAs
prov:wasDerivedFrom
foaf:isPrimaryTopicOf
is dbo:wikiPageRedirects of
is dbo:wikiPageWikiLink of
is foaf:primaryTopic of
Powered by OpenLink Virtuoso    This material is Open Knowledge     W3C Semantic Web Technology     This material is Open Knowledge    Valid XHTML + RDFa
This content was extracted from Wikipedia and is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License