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MYOCD

myocardin
2 disorders 1 untyped 1 causative 17p12 gene with protein product
HGNC:16067MonarchNCBI Gene 93649ENSG00000141052UniProt Q8IZQ8OMIM 606127

Aliases: MYCD.

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
Prune Belly Syndrome causative
mechanism: MYOCD-associated impaired smooth-muscle differentiation
Leiomyosarcoma untyped
Focal amplification

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