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CYP2D6*5 Allele

Go to external page http://purl.obolibrary.org/obo/NCIT_C45621

Human CYP2D6*5 allele is a variant form of the CYP2D6 wild-type allele. The CYP2D6*5 allele is a result of deletion of the entire CYP2D6 gene. Thus, the CYP2D6*5 allele does not encode a cytochrome P450 2D6 protein. This is the basis of the poor metabolizer phenotype in individuals who carry this allele. [ ]

Term info

Label

CYP2D6*5 Allele

Synonyms
  • CYP2D6 Deleted
  • CYP2D6*5
  • CYP2D6*5 Allele
  • CYP2D6, del
  • CYP2D6D
  • Cytochrome P450, Family 2, Subfamily D, Polypeptide 6*5 Allele
Subsets

NCIT_C116977, NCIT_C142800, NCIT_C142799

DesignNote

Ethnicity Association: Asian; African American; Black African; Caucasian; Middle Eastern

Display Name

CYP2D6*5 Allele

Legacy Concept Name

CYP2D6_5_Allele

OMIM Number

124030

Preferred Name

CYP2D6*5 Allele

PubMedID Primary Reference

8634695, 1673290

Semantic Type

Gene or Genome

UMLS CUI

C1707227

code

C45621