CARM1

Gene

coactivator associated arginine methyltransferase 1

HGNCHGNC:23393 EnsemblENSG00000142453 NCBI Gene10498

Locus: gene with protein productLocation: 19p13.2

Also known as

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

Also known asPRMT4

View full nomenclature history (1)

Alias symbolsPRMT4

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

Hypothyroidism

Lysosomal Storage Diseases

Mucositis

Stomatitis

Neurodevelopmental Disorders

Neoplasms

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.

7BS protein arginine methyltranferasesArginine methyltransferases

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.