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FMN1

Gene

formin 1

HGNCHGNC:3768EnsemblENSG00000248905NCBI Gene342184
Locus: gene with protein productLocation: 15q13.3

Also known as

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

Also known asLD · FMN · DKFZP686C2281 · FLJ45135 · MGC125288 · MGC125289
View full nomenclature history (8)
Previous symbolsLD, FMN
Alias symbolsDKFZP686C2281, FLJ45135, MGC125288, MGC125289
Previous namesformin (limb deformity)
Alias nameslimb deformity protein

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.

Cutaneous melanoma
Alopecia
Prostate carcinoma

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.

Formins

Provenance

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