About: CYP2C9*11 Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • CYP2C9*11 Allele
rdfs:subClassOf
OMIM_Number
  • 601130
GenBank_Accession_Number
  • NM_000771
Semantic_Type
  • Gene or Genome
Preferred_Name
  • CYP2C9*11 Allele
PubMedID_Primary_Reference
  • 11926893
  • 15284535
  • 15608560
UMLS_CUI
  • C1707197
Legacy_Concept_Name
  • CYP2C9_11_Allele
FULL_SYN
  • Cytochrome P450, Family 2, Subfamily C, Polypeptide 9*11 AlleleSYNCI
  • CYP2C9, R335WSYNCI
  • CYP2C9*11 AllelePTNCI
  • CYP2C9, c.1003C>TSYNCI
  • CYP2C9*11SYNCI
Gene_Encodes_Product
  • Cytochrome P450 2C9
DEFINITION
  • Human CYP2C9*11 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*11 protein. The CYP2C9*11 allele exhibits a clinically-relevant SNP (c.1003C>T) in exon 7 that results in a R335W coding change. This alteration in protein sequence severely decreases the enzymatic activity of the cytochrome P450 2C9*11 protein.NCI
DesignNote
  • Ethnicity Association: Black African
code
  • C46016
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