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NEGR1

Gene

neuronal growth regulator 1

HGNCHGNC:17302EnsemblENSG00000172260NCBI Gene257194
Locus: gene with protein productLocation: 1p31.1

Also known as

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

Also known asNtra · KILON · MGC46680 · IGLON4
View full nomenclature history (7)
Alias symbolsNtra, KILON, MGC46680, IGLON4
Alias namesa kindred of IgLON, neurotractin, IgLON family member 4

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.

Major depressive disorder
Intelligence
Obesity disorder
Autism Spectrum Disorder
Attention Deficit Disorder with Hyperactivity
Hair color
Bipolar Disorder
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.

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.