TSPYL4

Gene

TSPY like 4

HGNCHGNC:21559 EnsemblENSG00000187189 NCBI Gene23270

Locus: gene with protein productLocation: 6q22.1

Also known as

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

Also known asdJ486I3.2 · KIAA0721

View full nomenclature history (2)

Alias symbolsdJ486I3.2, KIAA0721

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.

Major depressive disorder

Depressive Disorder

Epilepsies, Myoclonic

Carcinoma, Non-Small-Cell Lung

Glioblastoma

Pulmonary Disease, Chronic Obstructive

Kidney Failure, Chronic

Colorectal adenocarcinoma

Intervertebral Disc Degeneration

Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy

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.

TSPYL family

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.