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NTNG1

Gene

netrin G1

HGNCHGNC:23319EnsemblENSG00000162631NCBI Gene22854
Locus: gene with protein productLocation: 1p13.3

Also known as

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

Also known asKIAA0976 · Lmnt1 · NetG1 · NetrinG1
View full nomenclature history (7)
Alias symbolsKIAA0976, Lmnt1, NetG1, NetrinG1
Alias namesnetrin G1f, Netrin-G1, laminet-1

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.

Obesity disorder
atypical Rett syndrome
Complex neurodevelopmental disorder
Overnutrition
Obesity, Morbid
Diabetes Mellitus, Type 2
Ovarian dysfunction
Liver Diseases

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.

Netrins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-05-02.
Open TargetsGene–disease associations from the Open Targets Platform.