Back to discover

SLC9D1

Gene

solute carrier family 9 member D1

HGNCHGNC:20329EnsemblENSG00000150403NCBI Gene55002
Locus: gene with protein productLocation: 13q34

Also known as

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

Also known asC13orf11 · TMCO3 · FLJ20623
View full nomenclature history (5)
Previous symbolsC13orf11, TMCO3
Alias symbolsFLJ20623
Previous namestransmembrane and coiled-coil domains 3, chromosome 13 open reading frame 11

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.

Pre-Eclampsia
Carcinoma, Hepatocellular
bone Paget's disease
Kallmann syndrome
Melorheostosis
Hypogonadism

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 9

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-07-09.
Open TargetsGene–disease associations from the Open Targets Platform.