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SLC25A23

Gene

solute carrier family 25 member 23

HGNCHGNC:19375EnsemblENSG00000125648NCBI Gene79085
Locus: gene with protein productLocation: 19p13.3

Also known as

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

Also known asFLJ30339 · MGC2615 · APC2
View full nomenclature history (4)
Alias symbolsFLJ30339, MGC2615, APC2
Previous namessolute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23

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.

Neurodegenerative Diseases
Hypertension, Portal
Tyrosinemias

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.

EF-hand domain containingSolute carrier family 25

Provenance

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