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PYCARD

PYD and CARD domain containing
2 disorders 1 untyped 1 no genetic record 16p11.2 gene with protein product
HGNC:16608MonarchNCBI Gene 29108ENSG00000103490UniProt Q9ULZ3OMIM 606838

Aliases: TMS-1, CARD5, ASC.

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
Alzheimer Disease untyped
Genetic Variant
mechanism: Neuroinflammation
Multiple Sclerosis no genetic record
mechanism: Microglial NLRP3 Inflammasome Activation
Mechanism modules · computed from kb/

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