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Literature summary for 1.14.14.16 extracted from

  • Trinh, L.; Nimkarn, S.; New, M.I.; Lin-Su, K.
    Growth and pubertal characteristics in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2007), J. Pediatr. Endocrinol. Metab., 20, 883-891.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
gene CYP11B!, DNA and amino acid sequence determination and analysis, genotyping Homo sapiens

Protein Variants

Protein Variants Comment Organism
additional information enzyme deficiency, i.e. 21-OHD, causes congenital adrenal hyperplasia, growth phenotypes of pubertal humans with salt wasting, simple virilizing, or non-classical 21-OHD, respectively, overview Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Homo sapiens enzyme deficiency, i.e. 21-OHD, causes congenital adrenal hyperplasia in pubertal subjects ?
-
?

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information enzyme deficiency, i.e. 21-OHD, causes congenital adrenal hyperplasia in pubertal subjects Homo sapiens ?
-
?

Synonyms

Synonyms Comment Organism
21-hydroxylase
-
Homo sapiens