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MYRF

Gene

myelin regulatory factor

HGNCHGNC:1181EnsemblENSG00000124920NCBI Gene745
Locus: gene with protein productLocation: 11q12.2

Also known as

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

Also known asC11orf9 · MRF · Ndt80 · pqn-47
View full nomenclature history (6)
Previous symbolsC11orf9
Alias symbolsMRF, Ndt80, pqn-47
Previous nameschromosome 11 open reading frame 9
Alias namesmyelin gene regulatory factor

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.

Genetic Diseases, Inborn
Microphthalmia

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.