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INF2

Gene

inverted formin 2

HGNCHGNC:23791EnsemblENSG00000203485NCBI Gene64423
Locus: gene with protein productLocation: 14q32.33

Also known as

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

Also known asC14orf151 · C14orf173 · MGC13251
View full nomenclature history (6)
Previous symbolsC14orf151, C14orf173
Alias symbolsMGC13251
Previous nameschromosome 14 open reading frame 151, chromosome 14 open reading frame 173, inverted formin, FH2 and WH2 domain containing

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
Kidney Diseases
Renal Insufficiency

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.

Armadillo like helical domain containingFormins

Provenance

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