ENSG00000185532


Homo sapiens

Features
Gene ID: ENSG00000185532
  
Biological name :PRKG1
  
Synonyms : PRKG1 / protein kinase, cGMP-dependent, type I / Q13976
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 10
Strand: 1
Band: q11.23
Gene start: 50990891
Gene end: 52298350
  
Corresponding Affymetrix probe sets: 207119_at (Human Genome U133 Plus 2.0 Array)   211380_s_at (Human Genome U133 Plus 2.0 Array)   228396_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000493966
Ensembl peptide - ENSP00000494124
Ensembl peptide - ENSP00000496551
Ensembl peptide - ENSP00000495279
Ensembl peptide - ENSP00000363087
Ensembl peptide - ENSP00000363092
Ensembl peptide - ENSP00000363097
Ensembl peptide - ENSP00000384200
NCBI entrez gene - 5592     See in Manteia.
OMIM - 176894
RefSeq - XM_017016412
RefSeq - XM_011539952
RefSeq - NM_001098512
RefSeq - NM_006258
RefSeq - XM_017016413
RefSeq Peptide - NP_006249
RefSeq Peptide - NP_001091982
swissprot - Q13976
swissprot - B1ALS0
swissprot - A0A0A0MSB3
Ensembl - ENSG00000185532
  
Related genetic diseases (OMIM): 615436 - Aortic aneurysm, familial thoracic 8, 615436
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 prkg1bENSDARG00000031702Danio rerio
 PRKG1ENSGALG00000003805Gallus gallus
 Prkg1ENSMUSG00000052920Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
PRKG2 / Q13237 / protein kinase, cGMP-dependent, type IIENSG0000013866952
P22694 / PRKACB / protein kinase cAMP-activated catalytic subunit betaENSG0000014287523
P17612 / PRKACA / protein kinase cAMP-activated catalytic subunit alphaENSG0000007206222
P22612 / PRKACG / protein kinase cAMP-activated catalytic subunit gammaENSG0000016505921
PRKX / P51817 / protein kinase, X-linkedENSG0000018394321


Protein motifs (from Interpro)
Interpro ID Name
 IPR000595  Cyclic nucleotide-binding domain
 IPR000719  Protein kinase domain
 IPR000961  AGC-kinase, C-terminal
 IPR002374  cGMP-dependent kinase
 IPR008271  Serine/threonine-protein kinase, active site
 IPR011009  Protein kinase-like domain superfamily
 IPR014710  RmlC-like jelly roll fold
 IPR017441  Protein kinase, ATP binding site
 IPR018488  Cyclic nucleotide-binding, conserved site
 IPR018490  Cyclic nucleotide-binding-like
 IPR031831  cGMP-dependent protein kinase, N-terminal coiled-coil domain
 IPR035014  cGMP-dependent protein kinase, catalytic domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001764 neuron migration IEA
 biological_processGO:0006468 protein phosphorylation IEA
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0008152 metabolic process IEA
 biological_processGO:0016310 phosphorylation IEA
 biological_processGO:0016358 dendrite development IEA
 biological_processGO:0019934 cGMP-mediated signaling IEA
 biological_processGO:0030036 actin cytoskeleton organization TAS
 biological_processGO:0030900 forebrain development IEA
 biological_processGO:0043087 regulation of GTPase activity IMP
 biological_processGO:0045986 negative regulation of smooth muscle contraction IEA
 biological_processGO:0060087 relaxation of vascular smooth muscle IEA
 biological_processGO:0090331 negative regulation of platelet aggregation IMP
 biological_processGO:1904706 negative regulation of vascular smooth muscle cell proliferation IDA
 biological_processGO:1904753 negative regulation of vascular associated smooth muscle cell migration IDA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005794 Golgi apparatus IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0005886 plasma membrane IEA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0004672 protein kinase activity IMP
 molecular_functionGO:0004674 protein serine/threonine kinase activity TAS
 molecular_functionGO:0004692 cGMP-dependent protein kinase activity IEA
 molecular_functionGO:0005246 calcium channel regulator activity IDA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0016301 kinase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0030553 cGMP binding IEA


Pathways (from Reactome)
Pathway description
Ca2+ pathway


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000023 Inguinal hernia 
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 HP:0000098 Increased body height 
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 HP:0000278 Retrognathia 
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 HP:0000316 Hypertelorism 
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 HP:0000525 Abnormality of the iris "An abnormality of the iris, which is the pigmented muscular tissue between the cornea and the lens, that is perforated by an opening called the pupil." [HPO:curators]
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 HP:0000766 Abnormality of the sternum 
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 HP:0000822 Hypertension "High blood pressure." [HPO:curators]
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 HP:0000965 Cutis marmorata 
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 HP:0000978 Ecchymoses 
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 HP:0001166 Arachnodactyly "Abnormally long and slender fingers ("spider fingers")." [HPO:curators]
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 HP:0001640 Cardiomegaly 
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 HP:0001643 Patent ductus arteriosus 
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 HP:0001647 Bicuspid aortic valve "The presence of a bicuspid `aortic valve` (FMA:7236)." [HPO:probinson]
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 HP:0001659 Aortic insufficiency "An insufficiency of the aortic valve, leading to regurgitation (backward flow) of blood from the aorta into the left ventricle." [HPO:curators]
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 HP:0001677 Coronary artery disease 
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 HP:0001763 Pes planus "A condition in which the arch of the foot is flat, with the entire sole of the foot being in near-complete contact with the ground." [HPO:curators]
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 HP:0002105 Hemoptysis "Coughing up (expectoration) of blood or blood-streaked sputum from the larynx, trachea, bronchi, or lungs." [HPO:curators]
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 HP:0002107 Pneumothorax 
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 HP:0002138 Subarachnoid hemorrhage 
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 HP:0002140 Ischemic stroke 
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 HP:0002326 Transient ischemic attack 
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 HP:0002616 Aortic root dilatation 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0002686 Prenatal maternal abnormality 
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 HP:0002705 High, narrow palate "The presence of a high and narrow palate." [HPO:curators]
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 HP:0002875 Exertional dyspnea 
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 HP:0004933 ascending aortic dissection 
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 HP:0004944 Cerebral aneurysm "The presence of a localized dilatation or ballooning of a cerebral artery." [HPO:curators]
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 HP:0004950 Peripheral arterial disease 
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 HP:0004959 Dilatation of the descending thoracic aorta 
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 HP:0005112 Dilatation of the abdominal aorta 
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 HP:0005162 Impaired left ventricular function 
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 HP:0006702 Spontaneous coronary artery dissection 
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 HP:0011106 Hypovolemia "An decrease in the amount of intravascular fluid, particularly in the volume of the circulating blood." [HPO:probinson]
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 HP:0012163 Carotid artery aneurysm "A aneurysm (balooning or bulging out of the vessel wall) of a carotid artery." [HPO:probinson]
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 HP:0012499 Descending aortic dissection "A separation of the layers within the wall of the `descending aorta` (FMA:3784). Tears in the intimal layer result in the propagation of dissection (proximally or distally) secondary to blood entering the intima-media space." [HPO:probinson]
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 HP:0012727 Thoracic aortic aneurysm "A bulging, weakened area in the wall of the thoracic aorta." [HPO:probinson]
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 HP:0012763 Paroxysmal dyspnea "A sudden attack of dyspnea that occurs while the affected person is at rest." [HPO:probinson]
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 HP:0030882 Coronary artery dilation 
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 HP:0100749 Chest pain 
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 HP:0100775 Dural ectasia "A widening or ballooning of the dural sac surrounding the spinal cord usually at the lumbosacral level." [HPO:sdoelken]
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 HP:0200146 Cystic medial necrosis of the aorta 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000150995 ITPR1 / Q14643 / inositol 1,4,5-trisphosphate receptor type 1  / reaction
 ENSG00000135643 KCNMB4 / Q86W47 / potassium calcium-activated channel subfamily M regulatory beta subunit 4  / reaction
 ENSG00000072952 MRVI1 / Q9Y6F6 / murine retrovirus integration site 1 homolog  / reaction
 ENSG00000156113 KCNMA1 / Q12791 / potassium calcium-activated channel subfamily M alpha 1  / reaction
 ENSG00000197584 KCNMB2 / Q9Y691 / potassium calcium-activated channel subfamily M regulatory beta subunit 2  / reaction
 ENSG00000132359 Q684P5 / RAP1GAP2 / RAP1 GTPase activating protein 2  / reaction
 ENSG00000171121 KCNMB3 / Q9NPA1 / potassium calcium-activated channel subfamily M regulatory beta subunit 3  / reaction
 ENSG00000185532 PRKG1 / Q13976 / protein kinase, cGMP-dependent, type I  / complex
 ENSG00000145936 KCNMB1 / Q16558 / potassium calcium-activated channel subfamily M regulatory beta subunit 1  / reaction






 

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