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Literature summary for 1.14.15.4 extracted from

  • Simm, P.J.; Zacharin, M.R.
    Successful pregnancy in a patient with severe 11-beta-hydroxylase deficiency and novel mutations in CYP11B1 gene (2007), Horm. Res., 68, 294-297.
    View publication on PubMed

Protein Variants

Protein Variants Comment Organism
additional information 11beta-hydroxylase deficiency caused by mutations inthe CYP11B1 gene can cause congenital adrenal hyperplasia, identification of mutations involved, biochemical androgen status of a mutant female during pregnancy and after delivery, overview Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Homo sapiens 11beta-hydroxylase deficiency is the second most common form of congenital adrenal hyperplasia after 21-hydroxylase deficiency, overview ?
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?

Organism

Organism UniProt Comment Textmining
Homo sapiens
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gene CYP11B1
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information 11beta-hydroxylase deficiency is the second most common form of congenital adrenal hyperplasia after 21-hydroxylase deficiency, overview Homo sapiens ?
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?

Synonyms

Synonyms Comment Organism
11-beta-hydroxylase
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Homo sapiens