CYP26B1 wt Allele

Human CYP26B1 wild-type allele is located in the vicinity of 2p13.2 and is approximately 19 kb in length. This allele, which encodes cytochrome P450 26B1 protein, is involved in the specific inactivation of all-trans-retinoic acid. Mutations in this gene are associated with craniofacial and other skeletal anomalies. (NCI Thesaurus)

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CYP26B1 Gene

This gene plays a role in the metabolism of retinoic acid.

CYP24A1 wt Allele

Human CYP24A1 wild-type allele is located within 20q13.2-q13.3 and is approximately 21 kb in length. This allele, which encodes 1,25-dihydroxyvitamin D(3) 24-hydroxylase,…

CYP24A1 Gene

This gene plays a role in vitamin D3 metabolism and calcium homeostasis.

CYP21A2 wt Allele

Human CYP21A2 wild-type allele is located in the vicinity of 6p21.3 and is approximately 3 kb in length. This allele, which encodes…

CYP21A2 Gene

This gene plays a role in steroid metabolism.

CYP1B1 wt Allele

Human CYP1B1 wild-type allele is located in the vicinity of 2p22.2 and is approximately 43 kb in length. This allele, which encodes…