SLC52A2

Gene

solute carrier family 52 member 2

HGNCHGNC:30224 EnsemblENSG00000185803 NCBI Gene79581

Locus: gene with protein productLocation: 8q24.3

Also known as

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

Also known asGPR172A · FLJ11856 · PAR1 · GPCR41 · D15Ertd747e · RFVT2 · hRFT3 · RFT3 · HuPAR-1

View full nomenclature history (13)

Previous symbolsGPR172A

Alias symbolsFLJ11856, PAR1, GPCR41, D15Ertd747e, RFVT2, hRFT3, RFT3, HuPAR-1

Previous namesG protein-coupled receptor 172A, solute carrier family 52 (riboflavin transporter), member 2

Alias namesG-protein coupled receptor 41, human porcine endogenous retrovirus subgroup A receptor 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

Hereditary sensory and autonomic neuropathy

Optic Atrophy, Hereditary, Leber

Optic Atrophy

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 52Flavoproteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.