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MED11

mediator complex subunit 11
2 disorders 2 untyped 17p13.2 gene with protein product
HGNC:32687MonarchNCBI Gene 400569ENSG00000161920UniProt Q9P086OMIM 612383

Aliases: HSPC296, MGC88387.

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
MED11-Related Disorder untyped
Causative
mechanism: MED11 complex-stability failure
Mediator Complex Neurodevelopmental Disorder untyped
Causative
mechanism: Core Module Disruption (Head, Structural, and Tail)
subtype: MED11
scoped to subtype: MED11

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