Browse All / Genes / CYP17A1

CYP17A1

cytochrome P450 family 17 subfamily A member 1
2 disorders 1 causative 1 untyped 10q24.32 gene with protein product
HGNC:2593MonarchNCBI Gene 1586ENSG00000148795UniProt P05093OMIM 609300

Previous symbols: CYP17. Aliases: P450C17, CPT7, S17AH.

Normal function · from ai-gene-review (P05093, commit 79fe13b38970) · AI-generated, not KB evidence

ai-gene-review has this gene at status INITIALIZED; the description is shown only once the review is complete. Read the draft upstream.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Congenital Adrenal Hyperplasia causative germline
mechanism: CYP17A1 17-Hydroxylase/17,20-Lyase Deficiency
subtype: 17A-OHD
scoped to subtype: 17A-OHD
Polycystic Ovary Syndrome untyped
Risk Factor

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.