Aliases: MLCK, smMLCK, MYLK1, MLCK1, KRP, Telokin, MLCK108, MLCK210, MYLK-L.
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 |
|---|---|---|
| Familial Thoracic Aortic Aneurysm and Aortic Dissection | causative germline |
mechanism: Vascular smooth muscle contractile apparatus disruption
subtype: MYLK-related
scoped to subtype: MYLK-related
|
| Idiopathic Gastroparesis | no genetic record |
mechanism: Smooth Muscle Contractile Protein and PDGFRA+ Cell Loss
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.