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FUZ

Gene

fuzzy planar cell polarity protein

HGNCHGNC:26219EnsemblENSG00000010361NCBI Gene80199
Locus: gene with protein productLocation: 19q13.33

Also known as

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

Also known asFLJ22688 · Fy · CPLANE3
View full nomenclature history (5)
Alias symbolsFLJ22688, Fy, CPLANE3
Previous namesfuzzy homolog (Drosophila)
Alias namesciliogenesis and planar polarity effector complex subunit 3

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.

Ciliopathy
Neural Tube Defects
Alzheimer's Disease
Lysosomal Storage Diseases
Multiple Sclerosis
Neurodegenerative Diseases
Parkinson's Disease
Amelogenesis imperfecta

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.

Ciliogenesis and planar polarity effector complex subunits

Provenance

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