About: CYP2C9*16 Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • CYP2C9*16 Allele
rdfs:subClassOf
OMIM_Number
  • 601130
GenBank_Accession_Number
  • NM_000771
Semantic_Type
  • Gene or Genome
Preferred_Name
  • CYP2C9*16 Allele
PubMedID_Primary_Reference
  • 15371982
UMLS_CUI
  • C1707199
Legacy_Concept_Name
  • CYP2C9_16_Allele
FULL_SYN
  • Cytochrome P450, Family 2, Subfamily C, Polypeptide 9*16 AlleleSYNCI
  • CYP2C9, T299ASYNCI
  • CYP2C9, c.895A>GSYNCI
  • CYP2C9*16 AllelePTNCI
  • CYP2C9*16SYNCI
Gene_Encodes_Product
  • Cytochrome P450 2C9
DEFINITION
  • Human CYP2C9*16 allele is located within 10q24 and is approximately 33 kb in length. This allele, a variant form of the CYP2C9 wild-type allele, encodes cytochrome P450 2C9*16 protein. The CYP2C9*16 allele exhibits a clinically-relevant SNP (c.895A>G) that results in a T299A coding change. This alteration in protein sequence decreases the in vivo enzymatic activity of the cytochrome P450 2C9*16 protein.NCI
DesignNote
  • Ethnicity Association: Asian
code
  • C46018
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