SLC68A1

Gene

solute carrier family 68 member 1

HGNCHGNC:26196 EnsemblENSG00000138111 NCBI Gene79847

Locus: gene with protein productLocation: 10q24.32

Also known as

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

Also known asC10orf77 · TMEM180 · MFSD13A · FLJ22529 · bA18I14.8

View full nomenclature history (7)

Previous symbolsC10orf77, TMEM180, MFSD13A

Alias symbolsFLJ22529, bA18I14.8

Previous namesmajor facilitator superfamily domain containing 13A, transmembrane protein 180

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.

Inflammatory Bowel Diseases

Schizophrenia

Childhood onset asthma

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 68

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-07-09.

Open TargetsGene–disease associations from the Open Targets Platform.