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PTPRD

Gene

protein tyrosine phosphatase receptor type D

HGNCHGNC:9668EnsemblENSG00000153707NCBI Gene5789
Locus: gene with protein productLocation: 9p24.1-p23

Also known as

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

Also known asPTPD · HPTP
View full nomenclature history (2)
Alias symbolsPTPD, HPTP

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.

Neurodegenerative Diseases
Sleep Initiation and Maintenance Disorders
Restless Legs Syndrome
Glaucoma, Open-Angle
Protozoan Infections
Ovarian neoplasm
Alzheimer's Disease
Stroke

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.

Fibronectin type III domain containingI-set domain containingProtein tyrosine phosphatases receptor typeLAR protein receptor tyrosine phosphatase 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.