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GUF1

Gene

GTP binding elongation factor GUF1

HGNCHGNC:25799EnsemblENSG00000151806NCBI Gene60558
Locus: gene with protein productLocation: 4p12

Also known as

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

Also known asFLJ13220
View full nomenclature history (3)
Alias symbolsFLJ13220
Previous namesGUF1 GTPase homolog (S. cerevisiae), GUF1 homolog, GTPase

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.

Infantile spasms
Hearing loss, autosomal recessive
Deafness
Sleep Initiation and Maintenance Disorders
Stomach Neoplasms

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.

Translational GTPases

Provenance

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