SLC35B3

Gene

solute carrier family 35 member B3

HGNCHGNC:21601 EnsemblENSG00000124786 NCBI Gene51000

Locus: gene with protein productLocation: 6p24.3

Also known as

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

Also known asC6orf196 · CGI-19 · dJ453H5.1 · PAPST2

View full nomenclature history (8)

Previous symbolsC6orf196

Alias symbolsCGI-19, dJ453H5.1, PAPST2

Previous nameschromosome 6 open reading frame 196, solute carrier family 35, member B3, solute carrier family 35 (adenosine 3'-phospho 5'-phosphosulfate transporter), member B3

Alias names3' phosphoadenosine 5' phosphosulfate transporter 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.

Smoking initiation

Obesity disorder

Cartilage Diseases

Oropharyngeal Neoplasms

Alopecia

Gastritis

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 35

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.