TGM5

transglutaminase 5

2 disorders 1 causative 1 modifier 15q15.2 gene with protein product

HGNC:11781 Monarch NCBI Gene 9333 ENSG00000104055 UniProt O43548 OMIM 603805

Aliases: TGX, TGMX.

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
Peeling Skin Syndrome	causative	mechanism: Crosslinking-enzyme deficiency in acral PSS subtype: APSS-TGM5 scoped to subtype: APSS-TGM5
Spinocerebellar Ataxia Type 1	modifier

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