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MED17

mediator complex subunit 17
2 disorders 2 untyped 11q21 gene with protein product
HGNC:2375MonarchNCBI Gene 9440ENSG00000042429UniProt Q9NVC6OMIM 603810

Previous symbols: CRSP6. Aliases: CRSP77, TRAP80, DRIP80, SRB4.

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
MED17-Related Disorder untyped
Causative
mechanism: MED17 head-module Mediator dysfunction
Mediator Complex Neurodevelopmental Disorder untyped
Causative
mechanism: Core Module Disruption (Head, Structural, and Tail)
subtype: MED17
scoped to subtype: MED17

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