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SLC41A2

Gene

solute carrier family 41 member 2

HGNCHGNC:31045EnsemblENSG00000136052NCBI Gene84102
Locus: gene with protein productLocation: 12q23.3

Also known as

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

Also known asDKFZP434K0427
View full nomenclature history (3)
Alias symbolsDKFZP434K0427
Previous namessolute carrier family 41, member 2, solute carrier family 41 (magnesium transporter), 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.

Pre-Eclampsia
Brugada syndrome
Familial progressive cardiac conduction defect
Atrial Fibrillation

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 41

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-12-17.
Open TargetsGene–disease associations from the Open Targets Platform.