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SLC35A1

Gene

solute carrier family 35 member A1

HGNCHGNC:11021EnsemblENSG00000164414NCBI Gene10559
Locus: gene with protein productLocation: 6q15

Also known as

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

Also known asCMPST · hCST · CMP-Sia-Tr
View full nomenclature history (6)
Alias symbolsCMPST, hCST, CMP-Sia-Tr
Previous namessolute carrier family 35 (UDP-galactose transporter), member 1, solute carrier family 35 (CMP-sialic acid transporter), member A1
Alias namesCMP-sialic acid transporter

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.

Congenital disorder of glycosylation
SRD5A3-congenital disorder of glycosylation
Atrial Fibrillation
Genetic Diseases, Inborn
Hypothyroidism

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.