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SLC25A22

Gene

solute carrier family 25 member 22

HGNCHGNC:19954EnsemblENSG00000177542NCBI Gene79751
Locus: gene with protein productLocation: 11p15.5

Also known as

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

Also known asNET44 · GC-1 · GC1 · FLJ13044 · EIEE3
View full nomenclature history (7)
Alias symbolsNET44, GC-1, GC1, FLJ13044, EIEE3
Previous namessolute carrier family 25 (mitochondrial carrier: glutamate), member 22
Alias namesEarly infantile epileptic encephalopathy 3

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.

Genetic developmental and epileptic encephalopathy
early-infantile DEE
Genetic Diseases, Inborn
Prostatic Neoplasms

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 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.