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NOB1

Gene

NIN1 (RPN12) binding protein 1 homolog

HGNCHGNC:29540EnsemblENSG00000141101NCBI Gene28987
Locus: gene with protein productLocation: 16q22.1

Also known as

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

Also known asPSMD8BP1 · NOB1P · ART-4 · MST158
View full nomenclature history (8)
Previous symbolsPSMD8BP1
Alias symbolsNOB1P, ART-4, MST158
Previous namesPSMD8 binding protein 1, NIN1/RPN12 binding protein 1 homolog (S. cerevisiae), NIN1/PSMD8 binding protein 1 homolog
Alias namesnin one binding protein

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.

Corneal Dystrophies, Hereditary
Neurodegenerative Diseases
Smoking behavior
Alzheimer's Disease
Risk-taking behaviour
Gout
Cataract
Intelligence

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.

EndoribonucleasesRibosome biogenesis factors

Provenance

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