SLC20A2

Gene

solute carrier family 20 member 2

HGNCHGNC:10947 EnsemblENSG00000168575 NCBI Gene6575

Locus: gene with protein productLocation: 8p11.21

Also known as

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

Also known asMLVAR · GLVR2 · Glvr-2 · PiT-2 · Ram-1 · PIT2

View full nomenclature history (10)

Previous symbolsMLVAR, GLVR2

Alias symbolsGlvr-2, PiT-2, Ram-1, PIT2

Previous namessolute carrier family 20 (phosphate transporter), member 2, murine leukemia virus, amphotropic; receptor

Alias namesSodium-dependent phosphate transporter 2, gibbon ape leukemia virus receptor 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.

Bilateral striopallidodentate calcinosis

Genetic Diseases, Inborn

Gout

Neurodegenerative Diseases

Narcolepsy

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 20

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.