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IFT57

Gene

intraflagellar transport 57

HGNCHGNC:17367EnsemblENSG00000114446NCBI Gene55081
Locus: gene with protein productLocation: 3q13.12-q13.13

Also known as

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

Also known asESRRBL1 · FLJ10147 · HIPPI · MHS4R2
View full nomenclature history (6)
Previous symbolsESRRBL1
Alias symbolsFLJ10147, HIPPI, MHS4R2
Previous namesestrogen-related receptor beta like 1, intraflagellar transport 57 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.

Bardet-Biedl Syndrome
Hypothyroidism
Smoking cessation
Nutritional deficiency disease
Neurodegenerative Diseases
Ciliopathy
Smoking initiation

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.

IFT-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.