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UBXN4

Gene

UBX domain protein 4

HGNCHGNC:14860EnsemblENSG00000144224NCBI Gene23190
Locus: gene with protein productLocation: 2q21.3

Also known as

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

Also known asUBXDC1 · UBXD2 · KIAA0242
View full nomenclature history (6)
Previous symbolsUBXDC1, UBXD2
Alias symbolsKIAA0242
Previous namesUBX domain containing 2, UBX domain-containing 2
Alias nameserasin

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
Essential Tremor
Obesity disorder
Metabolic Syndrome
Autosomal dominant macrothrombocytopenia
Sprain
Cutaneous lupus erythematosus

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.

UBX domain containing

Provenance

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