SLC25A19

Gene

solute carrier family 25 member 19

HGNCHGNC:14409 EnsemblENSG00000125454 NCBI Gene60386

Locus: gene with protein productLocation: 17q25.1

Also known as

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

Also known asMCPHA · TPC · DNC · MUP1

View full nomenclature history (10)

Previous symbolsMCPHA

Alias symbolsTPC, DNC, MUP1

Previous namessolute carrier family 25 (mitochondrial deoxynucleotide carrier), member 19, microcephaly, Amish, solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19

Alias namesMitochondrial thiamine pyrophosphate carrier, Deoxynucleotide carrier, mitochondrial uncoupling protein 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.

Genetic Diseases, Inborn

Carcinoma, Hepatocellular

Colorectal Neoplasms

Adrenal gland disorder

Neoplasms

Lupus Erythematosus, Systemic

Microcephaly

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.