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IFT56

Gene

intraflagellar transport 56

HGNCHGNC:21882EnsemblENSG00000105948NCBI Gene79989
Locus: gene with protein productLocation: 7q34

Also known as

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

Also known asTTC26 · FLJ12571 · dyf-13 · DYF13
View full nomenclature history (5)
Previous symbolsTTC26
Alias symbolsFLJ12571, dyf-13, DYF13
Previous namestetratricopeptide repeat domain 26

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.

Caroli Disease
Wounds and Injuries
Spermatogenic failure
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.

Tetratricopeptide repeat domain containingIFT-B1 complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-02-24.
Open TargetsGene–disease associations from the Open Targets Platform.