About: CYP3A5*9 Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • CYP3A5*9 Allele
rdfs:subClassOf
OMIM_Number
  • 605325
GenBank_Accession_Number
  • NM_000777
Semantic_Type
  • Gene or Genome
Preferred_Name
  • CYP3A5*9 Allele
PubMedID_Primary_Reference
  • 12398984
UMLS_CUI
  • C1707238
Legacy_Concept_Name
  • CYP3A5_9_Allele
FULL_SYN
  • Cytochrome P450, Family 3, Subfamily A, Polypeptide 5*9 AlleleSYNCI
  • CYP3A5, A337TSYNCI
  • CYP3A5*9 AllelePTNCI
  • CYP3A5, g.19386G>ASYNCI
  • CYP3A5*9SYNCI
Gene_Encodes_Product
  • Cytochrome P450 3A5
DEFINITION
  • Human CYP3A5*9 allele is located in the vicinity of 7q21.1 and is approximately 32 kb in length. This allele, a variant form of the human CYP3A5 wild-type allele, encodes cytochrome P450 3A5*9 protein. The CYP3A5*9 allele exhibits a clinically-relevant SNP (g.19386G>A) in exon 10 that results in an A337T coding change. This alteration in protein sequence decreases the enzymatic activity of the cytochrome P450 3A5*9 protein.NCI
DesignNote
  • Ethnicity Association: Asian
code
  • C46024
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