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steroid-11-hydroxylase-B2 gene or CYP11B2
Mutations in CYP11B2 are the cause of aldosterone deficiency 1
Related
cytochrome P450 11B2 (cytochrome P450 C18, CYPC18, steroid-11-hydroxylase B2, CYP11B2, aldosterone synthase, steroid 18-hydroxylase)
General
unclassified gene
Properties
TEMPLATE-FOR: messenger RNA
TEMPLATE-FOR: steroid-11-hydroxylase B2
LOCUS: human chromosome-8 Q21
SIZE: entity length = 9 EXONS
MOTIF: transcription factor binding site
transcriptional start site
exon
intron
transcriptional termination site
Database Correlations
OMIM 124080
References
OMIM :accession 124080