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P2RX1

Gene

purinergic receptor P2X 1

HGNCHGNC:8533EnsemblENSG00000108405NCBI Gene5023
Locus: gene with protein productLocation: 17p13.2

Also known as

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

Also known asP2X1
View full nomenclature history (2)
Alias symbolsP2X1
Previous namespurinergic receptor P2X, ligand-gated ion channel, 1

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.

Placental abruption
Platelet-type bleeding disorder 8
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Colitis
Leukemia, Myeloid, Acute
Spermatogenic failure
Non-syndromic male infertility due to sperm motility disorder

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.

Purinergic receptors P2X

Provenance

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