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FCHO1

Gene

FCH and mu domain containing endocytic adaptor 1

HGNCHGNC:29002EnsemblENSG00000130475NCBI Gene23149
Locus: gene with protein productLocation: 19p13.11

Also known as

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

Also known asKIAA0290
View full nomenclature history (2)
Alias symbolsKIAA0290
Previous namesFCH domain only 1

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.

Severe congenital neutropenia
Coronary Artery Disease
Myocardial Infarction
Amyotrophic Lateral Sclerosis
Cardiovascular Diseases
Neurodegenerative Diseases

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.

F-BAR 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.