Previous symbols: CDK11, CDC2L6. Aliases: KIAA1028, bA346C16.3.
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 |
|---|---|---|
| CDK19-Related Disorder |
causative
germline
G2P: strong
|
mechanism: CDK19 Coding Missense Substitutions; Impaired CDK19 Functional Complementation; Increased CDK19 Kinase Activity; Reduced CDK19 Kinase Activity
|
| Mediator Complex Neurodevelopmental Disorder |
untyped
Causative
|
mechanism: CDK8 Kinase Module Dysfunction
subtype: CDK19
scoped to subtype: CDK19
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.