Back to discover

IFT80

Gene

intraflagellar transport 80

HGNCHGNC:29262EnsemblENSG00000068885NCBI Gene57560
Locus: gene with protein productLocation: 3q25.33

Also known as

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

Also known asWDR56 · KIAA1374 · FAP167 · CFAP167
View full nomenclature history (6)
Previous symbolsWDR56
Alias symbolsKIAA1374, FAP167, CFAP167
Previous namesWD repeat domain 56, intraflagellar transport 80 homolog (Chlamydomonas)

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
Myeloproliferative disorder
Hypothyroidism

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.

WD repeat domain containingIFT-B2 complex

Provenance

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