Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10887
Gene name Gene Name - the full gene name approved by the HGNC.
Prokineticin receptor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PROKR1
Synonyms (NCBI Gene) Gene synonyms aliases
GPR73, GPR73a, PK-R1, PKR1, ZAQ
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p13.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the G-protein-coupled receptor family. The encoded protein binds to prokineticins (1 and 2), leading to the activation of MAPK and STAT signaling pathways. Prokineticins are protein ligands involved in angiogenesis and inflam
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs144018404 T>A Likely-pathogenic Coding sequence variant, missense variant
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IBA 21873635
GO:0004983 Function Neuropeptide Y receptor activity IEA
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0007186 Process G protein-coupled receptor signaling pathway IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607122 4524 ENSG00000169618
Protein
UniProt ID Q8TCW9
Protein name Prokineticin receptor 1 (PK-R1) (G-protein coupled receptor 73) (G-protein coupled receptor ZAQ) (GPR73a)
Protein function 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. Ma
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 79 342 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Localizes to glandular epithelium, stroma and vascular endothelial cells of first trimester decidua (at protein level). Up-regulated in first trimester decidua when compared with non-pregnant endometrium. Expressed in the stomach, thro
Sequence
Sequence length 393
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Peptide ligand-binding receptors
G alpha (q) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hirschsprung disease Hirschsprung Disease rs76262710, rs75996173, rs77316810, rs75076352, rs76534745, rs76764689, rs76449634, rs377767412, rs193922699, rs75030001, rs606231342, rs1553540620, rs759944122, rs1057519322, rs1057519323
View all (4 more)
Unknown
Disease term Disease name Evidence References Source
Ischemic Stroke Ischemic Stroke GWAS
Associations from Text Mining
Disease Name Relationship Type References
Abortion Habitual Associate 25064403
Abortion Spontaneous Associate 25064403
Adrenal Gland Diseases Associate 26475302
Adrenocortical Adenoma Associate 26475302
Fetal Growth Retardation Associate 22941044
Hirschsprung Disease Associate 21858136
Hypoxia Associate 22941044
Neoplasms Associate 26475302
Pregnancy Ectopic Associate 21224062