SLC35B1

Gene

solute carrier family 35 member B1

HGNCHGNC:20798 EnsemblENSG00000121073 NCBI Gene10237

Locus: gene with protein productLocation: 17q21.33

Also known as

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

Also known asUGTREL1 · AXER

View full nomenclature history (4)

Alias symbolsUGTREL1, AXER

Previous namessolute carrier family 35, member B1

Alias namesATP/ADP exchanger in the ER membrane

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.

Neurodegenerative Diseases

Myeloproliferative disorder

Heart Failure

Cholestasis, Intrahepatic

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.