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NIN

Gene

ninein

HGNCHGNC:14906EnsemblENSG00000100503NCBI Gene51199
Locus: gene with protein productLocation: 14q22.1

Also known as

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

View full nomenclature history (1)
Previous namesninein (GSK3B interacting 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.

Microcephalic primordial dwarfism
Seckel syndrome
Neurodegenerative Diseases
Hearing Loss
Gastric adenocarcinoma
Colorectal adenocarcinoma

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.

EF-hand domain containingCentriolar satellite proteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.