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NTM

Gene

neurotrimin

HGNCHGNC:17941EnsemblENSG00000182667NCBI Gene50863
Locus: gene with protein productLocation: 11q25

Also known as

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

Also known asHNT · NTRI · IGLON2 · CEPU-1
View full nomenclature history (6)
Alias symbolsHNT, NTRI, IGLON2, CEPU-1
Alias namesneurotrimin, IgLON family member 2

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.

Smoking initiation
Ovarian dysfunction
Refractive Errors
Placental abruption

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.

I-set domain containingIgLON cell adhesion molecules

Provenance

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