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SPATA2L

Gene

spermatogenesis associated 2 like

HGNCHGNC:28393EnsemblENSG00000158792NCBI Gene124044
Locus: gene with protein productLocation: 16q24.3

Also known as

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

Also known asC16orf76 · MGC26885 · tamo
View full nomenclature history (4)
Previous symbolsC16orf76
Alias symbolsMGC26885, tamo
Previous nameschromosome 16 open reading frame 76

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.

Sinusitis
Presbycusis
Alzheimer's Disease
Vitiligo
Melanoma
Pancreatic Neoplasms
Friedreich Ataxia

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.

Provenance

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