CYP3A4*17 Allele
Human CYP3A4*17 allele is located in the vicinity of 7q21.1 and is approximately 27 kb in length. This allele, a variant form of the CYP3A4 wild-type allele, encodes cytochrome P450 3A4*17 protein. The CYP3A4*17 allele exhibits a clinically-relevant SNP (g.15615T>C) in exon 7 that results in a F189S coding change. This alteration in protein sequence severely decreases the enzymatic activity of the cytochrome P450 3A4*17 protein. [ ]
Term info
CYP3A4*17 Allele
- CYP3A4*17
- CYP3A4*17 Allele
- CYP3A4, F189S
- CYP3A4, g.15615T>C
- Cytochrome P450, Family 3, Subfamily A, Polypeptide 4*17 Allele
NCIT_C116977, NCIT_C142800, NCIT_C142799
CTRP
Ethnicity Association: Asian
CYP3A4*17 Allele
NM_017460
Cytochrome P450 3A4
CYP3A4_17_Allele
124010
CYP3A4*17 Allele
11714865
rs4987161
Gene or Genome
C1707234
C46026
Term relations
- CYP3A4 Gene
- Allele_Plays_Altered_Role_In_Process some Drug Metabolism
- Allele_Plays_Altered_Role_In_Process some Xenobiotic Metabolism
- Allele_In_Chromosomal_Location some 7q22.1
- Allele_Has_Activity some Decreased Biochemical Activity
- Allele_Has_Abnormality some Transition Mutation
- Allele_Has_Abnormality some Thymidine to Cytosine Transition Abnormality