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PASK

Gene

PAS domain containing serine/threonine kinase

HGNCHGNC:17270EnsemblENSG00000115687NCBI Gene23178
Locus: gene with protein productLocation: 2q37.3

Also known as

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

Also known asPASKIN · KIAA0135 · STK37
View full nomenclature history (3)
Alias symbolsPASKIN, KIAA0135, STK37

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.

Autoimmune disorder of central nervous system
Ovarian dysfunction
Ovarian neoplasm
Pre-Eclampsia
Kidney Failure, Chronic
Adrenal Insufficiency
Carpal Tunnel Syndrome
autosomal dominant hyperinsulinism due to Kir6.2 deficiency

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.

PAS domain containingPASK family kinases

Provenance

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