CYP2C8*2 Allele
Human CYP2C8*2 allele is located in the vicinity of 10q23.33 and is approximately 33 kb in length. This allele, a variant form of the CYP2C8 wild-type allele, encodes cytochrome P450 2C8*2 protein. The CYP2C8*2 allele exhibits a clinically-relevant SNP (c.805A>T) in exon 5 that results in an I269F coding change. This sequence alteration in the cytochrome P450 2C8*2 protein increases the Km of this enzyme for paclitaxel, thereby decreasing the clearance of this drug. [ ]
Term info
CYP2C8*2 Allele
- CYP2C8*2
- CYP2C8*2 Allele
- CYP2C8, I269F
- CYP2C8, c.805A>T
- Cytochrome P450, Family 2, Subfamily C, Polypeptide 8*2 Allele
NCIT_C116977, NCIT_C142800, NCIT_C142799
CTRP
Ethnicity Association: African American
CYP2C8*2 Allele
NM_000770
Cytochrome P450 2C8
CYP2C8_2_Allele
601129
CYP2C8*2 Allele
11668219
rs11572103
Gene or Genome
C1707189
C46030
Term relations
- CYP2C8 Gene
- Allele_Plays_Altered_Role_In_Process some Drug Metabolism
- Allele_Has_Abnormality some Adenosine to Thymidine Transversion Abnormality
- Allele_Plays_Altered_Role_In_Process some Xenobiotic Metabolism
- Allele_In_Chromosomal_Location some 10q23.33
- Allele_Has_Abnormality some Transversion Mutation
- Allele_Has_Activity some Decreased Biochemical Activity