PROKR2 (prokineticin receptor 2)

2016-10-01  

Identity

HGNC
LOCATION
20p12.3
LOCUSID
ALIAS
GPR73L1,GPR73b,GPRg2,HH3,KAL3,PKR2,dJ680N4.3

Other Information

Locus ID:

NCBI: 128674
MIM: 607123
HGNC: 15836
Ensembl: ENSG00000101292

Variants:

dbSNP: 128674
ClinVar: 128674
TCGA: ENSG00000101292
COSMIC: PROKR2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000101292ENST00000217270Q8NFJ6

Expression (GTEx)

0
1

Pathways

PathwaySourceExternal ID
Signal TransductionREACTOMER-HSA-162582
Signaling by GPCRREACTOMER-HSA-372790
GPCR ligand bindingREACTOMER-HSA-500792
Class A/1 (Rhodopsin-like receptors)REACTOMER-HSA-373076
Peptide ligand-binding receptorsREACTOMER-HSA-375276
GPCR downstream signalingREACTOMER-HSA-388396
G alpha (q) signalling eventsREACTOMER-HSA-416476
Gastrin-CREB signalling pathway via PKC and MAPKREACTOMER-HSA-881907

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
170543992006Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.132
185599222008Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.77
203796142010Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.62
124275522002Molecular cloning and characterization of prokineticin receptors.55
200229912010A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes.42
200229912010A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes.42
186825032008Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.39
186825032008Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.39
207340642010A large-scale candidate gene association study of age at menarche and age at natural menopause.38
188269632009PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity.36

Citation

Dessen P

PROKR2 (prokineticin receptor 2)

Atlas Genet Cytogenet Oncol Haematol. 2016-10-01

Online version: http://atlasgeneticsoncology.org/gene/56318/prokr2