Homo sapiens cytochrome P450 family 26 subfamily B member 1 (CYP26B1), - Nucleotide

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CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence. [Hum Genet. 2023]
CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence.
Silveira KC, Fonseca IC, Oborn C, Wengryn P, Ghafoor S, Beke A, Dreseris ES, Wong C, Iacovone A, Soltys CL, et al. Hum Genet. 2023 Nov; 142(11):1571-1586. Epub 2023 Sep 27.
Familial monoallelic CYP26B1 truncating variant causes a syndromic craniosynostosis due to haploinsufficiency ? [Eur J Med Genet. 2023]
Familial monoallelic CYP26B1 truncating variant causes a syndromic craniosynostosis due to haploinsufficiency ?
Sarma AS, Peter Mathew R, Dalal A, Bhat V, Patil SJ. Eur J Med Genet. 2023 Jul; 66(7):104772. Epub 2023 Apr 24.
A variant in CYP26B1 associated with esophageal squamous cell carcinoma risk by affecting retinoic acid metabolism. [Mol Carcinog. 2023]
A variant in CYP26B1 associated with esophageal squamous cell carcinoma risk by affecting retinoic acid metabolism.
Niu S, Shi K, Yue X, Pan M, Song L, Gu L, Tan Y, Miao X, Tian J, Chang J. Mol Carcinog. 2023 Jul; 62(7):991-1000. Epub 2023 Apr 12.

RefSeq alternative splicing
See 12 reference mRNA sequence splice variants for the CYP26B1 gene.
RefSeq protein product
See the reference protein sequence for cytochrome P450 26B1 isoform 1 (NP_063938.1).

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Protein sequence from Nucleotide coding region
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Nucleotide