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PDXP

Gene

pyridoxal phosphatase

HGNCHGNC:30259EnsemblENSG00000241360NCBI Gene57026
Locus: gene with protein productLocation: 22q13.1

Also known as

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

Also known asdJ37E16.5 · FLJ32703 · CIN
View full nomenclature history (5)
Alias symbolsdJ37E16.5, FLJ32703, CIN
Previous namespyridoxal (pyridoxine, vitamin B6) phosphatase
Alias nameschronophin

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.

Neoplasms
Glioblastoma
Congenital myasthenic syndromes
congenital myopathy 7A, myosin storage, autosomal dominant

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.

HAD Asp-based protein 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.