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IFT46

Gene

intraflagellar transport 46

HGNCHGNC:26146EnsemblENSG00000118096NCBI Gene56912
Locus: gene with protein productLocation: 11q23.3

Also known as

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

Also known asC11orf60 · C11orf2 · FLJ21827 · FAP32 · CFAP32
View full nomenclature history (8)
Previous symbolsC11orf60
Alias symbolsC11orf2, FLJ21827, FAP32, CFAP32
Previous namesintraflagellar transport 46 homolog (Chlamydomonas), chromosome 11 open reading frame 60
Alias namescilia and flagella associated protein 32

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.

Psoriasis
Kartagener Syndrome
Ciliopathy
Polycystic Kidney Diseases
Dementia
Diabetes Mellitus
Obesity due to melanocortin 4 receptor deficiency

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.

Cilia and flagella associatedIFT-B1 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.