Homo sapiens Protein: C12orf39
Summary
InnateDB Protein IDBP-22942.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C12orf39
Protein Name chromosome 12 open reading frame 39
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000256969
InnateDB Gene IDBG-22940 (C12orf39)
Protein Structure
UniProt Annotation
Function Plays a role as a central modulator of cardiovascular and renal function and nociception. Plays also a role in energy metabolism and storage. Inhibits adrenocortical cell proliferation with minor stimulation on corticosteroid release (By similarity). {ECO:0000250}.Spexin-1: Intracerebroventricular administration of the peptide induces an increase in arterial blood pressure, a decrease in both heart rate and renal excretion and delayed natriuresis. Intraventricular administration of the peptide induces antinociceptive activity. Also induces contraction of muscarinic- like stomach smooth muscles. Intraperitoneal administration of the peptide induces a reduction in food consumption and body weight. Inhibits long chain fatty acid uptake into adipocytes (By similarity). Acts as a ligand for galanin receptors GALR2 and GALR3 (PubMed:17284679, PubMed:24517231). {ECO:0000250, ECO:0000269PubMed:17284679, ECO:0000269PubMed:24517231}.Spexin-2: Intracerebroventricular administration of the peptide induces a decrease in heart rate, but no change in arterial pressure, and an increase in urine flow rate. Intraventricular administration of the peptide induces antinociceptive activity (By similarity). {ECO:0000250}.
Subcellular Localization Secreted. Secreted, extracellular space. Cytoplasmic vesicle, secretory vesicle. Note=Secreted via the classical ER/Golgi-dependent pathway into the extracellular medium largely as a full-length protein without the signal peptide, and not as a hydrolyzed and amidated peptide (PubMed:19193193 and PubMed:17284679). Localized extracellularly surrounding the villous trophoblastic cells. Detected in the serum.
Disease Associations
Tissue Specificity Expressed in the type I glomic cells within the carotid body (at protein level). Expressed predominantly in pancreas, testis, kidney, brain and placenta. Expressed in submucosal layer of esophagus and stomach fundus. {ECO:0000269PubMed:17284679, ECO:0000269PubMed:19132080, ECO:0000269PubMed:19193193, ECO:0000269PubMed:23080164}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005184 neuropeptide hormone activity
GO:0031765 type 2 galanin receptor binding
GO:0031766 type 3 galanin receptor binding
Biological Process
GO:0003084 positive regulation of systemic arterial blood pressure
GO:0010459 negative regulation of heart rate
GO:0032099 negative regulation of appetite
GO:0035814 negative regulation of renal sodium excretion
GO:0044539 long-chain fatty acid import
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0051930 regulation of sensory perception of pain
Cellular Component
GO:0005615 extracellular space
GO:0030133 transport vesicle
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9BT56
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 80763
UniGene Hs.736260
RefSeq NP_085049
HUGO HGNC:28139
OMIM
CCDS CCDS31757
HPRD 14405
IMGT
EMBL AK027273 AK075342 BC004336 CH471094
GenPept AAH04336 BAG51298 BAG52117 EAW96444