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Table 2 Multiple sequence alignment of a segment of the CYP11B2 gene

From: The clinical significance of aldosterone synthase deficiency: report of a novel mutation in the CYP11B2 gene

Homo sapiens

GSVDTTAFPLLMT LFELARNPDV

Canis lupus

GSVDTTAYPLWMT LFELARNPDV

Mus musculus

GSVDTTAIPLVMT LFELARNPDV

Macaca mulatta

GSVDTTAFPLLMT LFELARNPDV

Rattus norvegicus

GSVDTTAIPLVMT LFELARNPDV

  1. Codon 326 of the CYP11B2 gene in homo sapiens and the corresponding codon in other species are in bold phase. The threonine residue at codon 326 (in bold) is highly conserved across different mammal species.
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BMC Endocrine Disorders

ISSN: 1472-6823

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