PROK2 (prokineticin 2)

2008-09-01  

Identity

HGNC
LOCATION
3p13
LOCUSID
ALIAS
BV8,HH4,KAL4,MIT1,PK2

Other Information

Locus ID:

NCBI: 60675
MIM: 607002
HGNC: 18455
Ensembl: ENSG00000163421

Variants:

dbSNP: 60675
ClinVar: 60675
TCGA: ENSG00000163421
COSMIC: PROK2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000163421ENST00000295619Q9HC23
ENSG00000163421ENST00000353065Q9HC23

Expression (GTEx)

0
50
100
150
200
250

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
120242062002Prokineticin 2 transmits the behavioural circadian rhythm of the suprachiasmatic nucleus.196
170543992006Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.132
179597742007Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.92
179033082007Genome-wide association of sleep and circadian phenotypes.87
185599222008Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.77
155486112004Bv8 and endocrine gland-derived vascular endothelial growth factor stimulate hematopoiesis and hematopoietic cell mobilization.59
126047922003The endocrine-gland-derived VEGF homologue Bv8 promotes angiogenesis in the testis: Localization of Bv8 receptors to endothelial cells.54
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

Citation

Dessen P

PROK2 (prokineticin 2)

Atlas Genet Cytogenet Oncol Haematol. 2008-09-01

Online version: http://atlasgeneticsoncology.org/gene/50357/prok2