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SPNS1

Gene

SPNS lysolipid transporter 1, lysophospholipid

HGNCHGNC:30621EnsemblENSG00000169682NCBI Gene83985
Locus: gene with protein productLocation: 16p11.2

Also known as

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

Also known asHSpin1 · nrs · SPINL · PP2030 · SPIN1 · LAT · SLC63A1
View full nomenclature history (10)
Alias symbolsHSpin1, nrs, SPINL, PP2030, SPIN1, LAT, SLC63A1
Previous namesspinster homolog 1 (Drosophila), sphingolipid transporter 1 (putative)
Alias namessolute carrier family 63 member 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.

Attention Deficit Disorder with Hyperactivity
Hypertrophy, Left Ventricular
Atrial Fibrillation

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 63, sphingosine phosphate transporters

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-14.
Open TargetsGene–disease associations from the Open Targets Platform.