PRMT6

Gene

protein arginine methyltransferase 6

HGNCHGNC:18241 EnsemblENSG00000198890 NCBI Gene55170

Locus: gene with protein productLocation: 1p13.3

Also known as

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

Also known asHRMT1L6 · FLJ10559

View full nomenclature history (3)

Previous symbolsHRMT1L6

Alias symbolsFLJ10559

Previous namesHMT1 hnRNP methyltransferase-like 6 (S. cerevisiae)

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.

Obesity disorder

Restless Legs Syndrome

Diabetes Mellitus, Type 2

Overnutrition

Sleep Initiation and Maintenance Disorders

Asthma

Drug Hypersensitivity

Movement Disorders

Sleep disorder

bone Paget's disease

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.