MED12L

Gene

mediator complex subunit 12L

HGNCHGNC:16050 EnsemblENSG00000144893 NCBI Gene116931

Locus: gene with protein productLocation: 3q25.1

Also known as

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

Also known asKIAA1635 · TNRC11L · TRALPUSH · TRALP

View full nomenclature history (6)

Alias symbolsKIAA1635, TNRC11L, TRALPUSH, TRALP

Previous namesmediator of RNA polymerase II transcription, subunit 12 homolog (S. cerevisiae)-like, mediator complex subunit 12 like

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.

Platelet-type bleeding disorder 8

Genetic Diseases, Inborn

Complex neurodevelopmental disorder

Smoking initiation

Neurodegenerative Diseases

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.