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PROKR2

Gene

prokineticin receptor 2

HGNCHGNC:15836EnsemblENSG00000101292NCBI Gene128674
Locus: gene with protein productLocation: 20p12.3

Also known as

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

Also known asGPR73L1 · KAL3 · GPR73b · PKR2 · GPRg2 · dJ680N4.3
View full nomenclature history (8)
Previous symbolsGPR73L1, KAL3
Alias symbolsGPR73b, PKR2, GPRg2, dJ680N4.3
Previous namesG protein-coupled receptor 73-like 1, Kallmann syndrome 3 (autosomal dominant)

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.

Kallmann syndrome
Hypogonadism
Hirschsprung disease
Hypogonadotropic hypogonadism 2 with or without anosmia
Genetic Diseases, Inborn

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.

Prokineticin receptors

Provenance

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