Browse All / Genes / MYL4

MYL4

myosin light chain 4
2 disorders 2 causative 17q21.32 gene with protein product
HGNC:7585MonarchNCBI Gene 4635ENSG00000198336UniProt P12829OMIM 160770

Aliases: ALC1, AMLC, GT1, PRO1957.

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
Atrial Standstill causative germline
mechanism: MYL4 Loss of Function
Familial Atrial Fibrillation causative germline
mechanism: Atrial Ion-Channel or Coupling Variant
subtype: MYL4-related
scoped to subtype: MYL4-related
Mechanism modules · computed from kb/

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