Homo sapiens cytochrome P450 family 21 subfamily A member 2 (CYP21A2), - Nucleotide

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Relation between HLA and copy number variation of steroid 21-hydroxylase in a Swedish cohort of patients with autoimmune Addison's disease. [Eur J Endocrinol. 2023]
Relation between HLA and copy number variation of steroid 21-hydroxylase in a Swedish cohort of patients with autoimmune Addison's disease.
Lundtoft C, Eriksson D, Bianchi M, Aranda-Guillén M, Landegren N, Rantapää-Dahlqvist S, Söderkvist P, Meadows JRS, DISSECT Consortium, ImmunoArray Consortium, et al. Eur J Endocrinol. 2023 Aug 2; 189(2):235-241.
The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes. [Front Endocrinol (Lausanne). 2...]
The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes.
Fanis P, Skordis N, Toumba M, Picolos M, Tanteles GA, Neocleous V, Phylactou LA. Front Endocrinol (Lausanne). 2023; 14:1156616. Epub 2023 May 31.
Tenascins and osteopontin in biological response in cornea. [Ocul Surf. 2023]
Tenascins and osteopontin in biological response in cornea.
Sumioka T, Matsumoto KI, Reinach PS, Saika S. Ocul Surf. 2023 Jul; 29:131-149. Epub 2023 May 18.

RefSeq alternative splicing
See 7 reference mRNA sequence splice variants for the CYP21A2 gene.

Protein
Protein sequence from Nucleotide coding region
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Nucleotide