STYXL1

Gene

serine/threonine/tyrosine interacting like 1

HGNCHGNC:18165 EnsemblENSG00000127952 NCBI Gene51657

Locus: gene with protein productLocation: 7q11.23

Also known as

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

Also known asDUSP24 · MK-STYX

View full nomenclature history (3)

Previous symbolsDUSP24

Alias symbolsMK-STYX

Previous namesdual specificity phosphatase 24 (putative)

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.

Substance-Related Disorders

Genetic Diseases, Inborn

Opioid-Related Disorders

Spermatogenic failure

Non-syndromic male infertility due to sperm motility disorder

Coffee consumption

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.

MAP kinase phosphatases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.