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SLC44A1

Gene

solute carrier family 44 member 1

HGNCHGNC:18798EnsemblENSG00000070214NCBI Gene23446
Locus: gene with protein productLocation: 9q31.1-q31.2

Also known as

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

Also known asCDW92 · CTL1 · CHTL1 · CD92
View full nomenclature history (7)
Previous symbolsCDW92
Alias symbolsCTL1, CHTL1, CD92
Previous namesCDW92 antigen, solute carrier family 44 (choline transporter), member 1
Alias namesCholine transporter-like protein 1

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.

Hyperaldosteronism
Neurodevelopmental Disorders
Metabolic Diseases
Placental abruption
Osteoarthritis, Knee

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.

CD moleculesSolute carrier family 44

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.