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MED16

mediator complex subunit 16
2 disorders 2 untyped 19p13.3 gene with protein product
HGNC:17556MonarchNCBI Gene 10025ENSG00000175221UniProt Q9Y2X0OMIM 604062

Previous symbols: THRAP5. Aliases: DRIP92, TRAP95.

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
Guillouet-Gordon Syndrome untyped
Causative
mechanism: MED16 Mediator mislocalization
Mediator Complex Neurodevelopmental Disorder untyped
Causative
mechanism: Core Module Disruption (Head, Structural, and Tail)
subtype: MED16
scoped to subtype: MED16

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