Skip to content
GenoLensGenoLens

PROKR1

Chr 2p13.3

prokineticin receptor 1

Aliases:
PKR1, ZAQ, GPR73a
MANE:
ENST00000303786.5

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Paediatric pseudo-obstruction syndrome

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Disease associations (Open Targets)

  • Hirschsprung disease

    0.44
  • Aganglionic megacolon

    0.26
  • retinitis pigmentosa

    0.12
  • Progressive cone dystrophy

    0.11
  • Cone rod dystrophy

    0.09
  • Oguchi disease

    0.08
  • Familial drusen

    0.08
  • neoplasm

    0.08
  • adult-onset foveomacular vitelliform dystrophy

    0.08
  • Familial exudative vitreoretinopathy

    0.08

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Prokineticin receptor 1

Receptor for prokineticin 1. Exclusively coupled to the G(q) subclass of heteromeric G proteins. Activation leads to mobilization of calcium, stimulation of phosphoinositide turnover and activation of p44/p42 mitogen-activated protein kinase. May play a role during early pregnancy

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.