MED7

Gene

mediator complex subunit 7

HGNCHGNC:2378 EnsemblENSG00000155868 NCBI Gene9443

Locus: gene with protein productLocation: 5q33.3

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asCRSP9 · CRSP33

View full nomenclature history (3)

Previous symbolsCRSP9

Alias symbolsCRSP33

Previous namescofactor required for Sp1 transcriptional activation, subunit 9, 33kDa

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Neurodegenerative Diseases

Gastritis, Atrophic

Thyroid Diseases

Hashimoto's Disease

Carcinoma, Hepatocellular

Neoplasms

Hypothyroidism

Infections

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Mediator complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.