About: CYP2C9*8 Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • CYP2C9*8 Allele
rdfs:subClassOf
OMIM_Number
  • 601130
GenBank_Accession_Number
  • NM_000771
Semantic_Type
  • Gene or Genome
Preferred_Name
  • CYP2C9*8 Allele
PubMedID_Primary_Reference
  • 15284535
UMLS_CUI
  • C1707206
SNP_ID
  • rs7900194
Legacy_Concept_Name
  • CYP2C9_8_Allele
FULL_SYN
  • Cytochrome P450, Family 2, Subfamily C, Polypeptide 9*8 AlleleSYNCI
  • CYP2C9, R150HSYNCI
  • CYP2C9*8 AllelePTNCI
  • CYP2C9, c.449G>ASYNCI
  • CYP2C9*8SYNCI
Gene_Encodes_Product
  • Cytochrome P450 2C8
DEFINITION
  • Human CYP2C9*8 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*8 protein. The CYP2C9*8 allele exhibits a clinically-relevant SNP (c.449G>A) in exon 3 that results in a R150H coding change. This alteration in protein sequence increases the enzymatic activity of the cytochrome P450 2C9*8 protein.NCI
DesignNote
  • Ethnicity Association: African American; Black African
code
  • C46015
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