PIEZO2

piezo type mechanosensitive ion channel component 2

2 disorders 1 causative 1 untyped 18p11.22-p11.21 gene with protein product

HGNC:26270 Monarch NCBI Gene 63895 ENSG00000154864 UniProt Q9H5I5 OMIM 613629

Previous symbols: FAM38B2, C18orf30, C18orf58, FAM38B. Aliases: FLJ23403, FLJ23144, HsT748, HsT771, FLJ34907.

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.

Disorder	Relationship	Where the gene appears
Gordon Syndrome	causative germline gain of function	mechanism: PIEZO2 Gain-of-Function and Mechanotransduction Defect
Marden-Walker Syndrome	untyped Causative

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