CYP2C9*5 Allele
Human CYP2C9*5 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*5 protein. The CYP2C9*5 allele exhibits a clinically-relevant SNP (c.1080C>G) in exon 7 that results in a D360E coding change. This alteration in the cytochrome P450 2C9*5 protein sequence increases the Km of this enzyme for (S)-warfarin, diclofenac, and lauric acid, thereby decreasing clearance of these drugs. [ ]
Term info
CYP2C9*5 Allele
- CYP2C9*5
- CYP2C9*5 Allele
- CYP2C9, D360E
- CYP2C9, c.1080C>G
- Cytochrome P450, Family 2, Subfamily C, Polypeptide 9*5 Allele
NCIT_C116977, NCIT_C142800, NCIT_C142799
CTRP
Ethnicity Association: African American
CYP2C9*5 Allele
NM_000771
Cytochrome P450 2C9
CYP2C9_5_Allele
601130
CYP2C9*5 Allele
15289788
Gene or Genome
C1707204
C45615
Term relations
- CYP2C9 Gene
- Allele_Plays_Altered_Role_In_Process some Drug Metabolism
- Allele_Has_Abnormality some Cytosine to Guanosine Transversion Abnormality
- Allele_Plays_Altered_Role_In_Process some Xenobiotic Metabolism
- Allele_Has_Abnormality some Transversion Mutation
- Allele_Has_Activity some Decreased Biochemical Activity
- Allele_In_Chromosomal_Location some 10q24