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NUP133

Gene

nucleoporin 133

HGNCHGNC:18016EnsemblENSG00000069248NCBI Gene55746
Locus: gene with protein productLocation: 1q42.13

Also known as

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

Also known asFLJ10814
View full nomenclature history (2)
Alias symbolsFLJ10814
Previous namesnucleoporin 133kDa

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.

Nephrotic Syndrome
HIV Infections
Influenza, Human
Virus Diseases
COVID-19
Diabetes Mellitus
Diabetes Mellitus, Type 2

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.

Minor histocompatibility antigensNucleoporins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-06-19.
Open TargetsGene–disease associations from the Open Targets Platform.