NIPAL3

Gene

NIPA like domain containing 3

HGNCHGNC:25233 EnsemblENSG00000001461 NCBI Gene57185

Locus: gene with protein productLocation: 1p36.11

Also known as

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

Also known asNPAL3 · DJ462O23.2 · SLC57A5

View full nomenclature history (3)

Previous symbolsNPAL3

Alias symbolsDJ462O23.2, SLC57A5

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.

Cutaneous melanoma

Hair color

Dyspepsia

Nervous System Diseases

Neurodevelopmental Disorders

Prostate carcinoma

Isolated agammaglobulinemia

Common variable immunodeficiency

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.

Solute carrier family 57, NIPA-like magnesium transporters

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-14.

Open TargetsGene–disease associations from the Open Targets Platform.