PROK2

Gene Information
 
Gene Symbol
PROK2
 
Aliases
BV8, HH4, KAL4, MIT1, PK2
 
Entrez Gene ID
 
Gene Name
Prokineticin 2
 
Chromosomal Location
3p13
 
HGNC ID
 
Summary
This gene encodes a protein expressed in the suprachiasmatic nucleus (SCN) circadian clock that may function as the output component of the circadian clock. The secreted form of the encoded protein may also serve as a chemoattractant for neuronal precursor cells in the olfactory bulb. Proteins from other vertebrates which are similar to this gene product were isolated based on homology to snake venom and secretions from frog skin, and have been shown to have diverse functions. Mutations in this gene are associated with Kallmann syndrome 4. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0000187 Biological process Activation of MAPK activity IBA 21873635
GO:0000187 Biological process Activation of MAPK activity TAS 12728244
GO:0001525 Biological process Angiogenesis IDA 12604792
GO:0006935 Biological process Chemotaxis IDA 12604792
GO:0006954 Biological process Inflammatory response NAS 11259612
Protein Information
 
Protein Name
Prokineticin-2, protein Bv8 homolog
 
Function
May function as an output molecule from the suprachiasmatic nucleus (SCN) that transmits behavioral circadian rhythm. May also function locally within the SCN to synchronize output. Potently contracts gastrointestinal (GI) smooth muscle
 
Refseq Proteins
 
UniProt
 
Pfam
Pfam Accession Pfam ID
PF06607 Prokineticin
Pathways
 
Reactome
 

 

Peptide ligand-binding receptors
G alpha (q) signalling events

Interactions
 
STRING MINT IntAct
ENSP00000295619 Q9HC23
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Cardiovascular Diseases
Aortic Aneurysm
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital heart disease
Anosmia
Stalk Interruption Syndrome
Developmental Delay
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
 
PCOS, Inflammation 
 
Rotterdam Criteria 
Direct 
8 PCOS Subjects and 8 Controls 
We conducted the peripheral-blood transcriptome in PCOS using microarray and identified dysregulated genes involved in inflammatory response. Our data strongly supported the notion that systemic rather than a local inflammatory response is implicated in the etiology of PCOS. 

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