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FRMD6

Gene

FERM domain containing 6

HGNCHGNC:19839EnsemblENSG00000139926NCBI Gene122786
Locus: gene with protein productLocation: 14q22.1

Also known as

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

Also known asC14orf31 · MGC17921 · willin · EX1
View full nomenclature history (6)
Previous symbolsC14orf31
Alias symbolsMGC17921, willin, EX1
Previous nameschromosome 14 open reading frame 31
Alias namesexpanded homolog

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
Dyspepsia
Scoliosis
Diabetes Mellitus
Adverse effect

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.

FERM domain containing

Provenance

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