ENSG00000065534


Homo sapiens

Features
Gene ID: ENSG00000065534
  
Biological name :MYLK
  
Synonyms : MYLK / myosin light chain kinase / Q15746
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 3
Strand: -1
Band: q21.1
Gene start: 123610049
Gene end: 123884331
  
Corresponding Affymetrix probe sets: 1563466_at (Human Genome U133 Plus 2.0 Array)   1568770_at (Human Genome U133 Plus 2.0 Array)   1569956_at (Human Genome U133 Plus 2.0 Array)   202555_s_at (Human Genome U133 Plus 2.0 Array)   224823_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000462118
Ensembl peptide - ENSP00000428967
Ensembl peptide - ENSP00000463691
Ensembl peptide - ENSP00000320622
Ensembl peptide - ENSP00000346846
Ensembl peptide - ENSP00000352088
Ensembl peptide - ENSP00000353452
Ensembl peptide - ENSP00000354004
Ensembl peptide - ENSP00000417798
Ensembl peptide - ENSP00000418335
Ensembl peptide - ENSP00000422984
NCBI entrez gene - 4638     See in Manteia.
OMIM - 600922
RefSeq - XM_017006473
RefSeq - NM_001321309
RefSeq - NM_053025
RefSeq - NM_053026
RefSeq - NM_053027
RefSeq - NM_053028
RefSeq - NM_053031
RefSeq - NM_053032
RefSeq - XM_011512860
RefSeq - XM_011512861
RefSeq - XM_017006472
RefSeq Peptide - NP_444253
RefSeq Peptide - NP_444254
RefSeq Peptide - NP_444255
RefSeq Peptide - NP_444256
RefSeq Peptide - NP_444259
RefSeq Peptide - NP_444260
RefSeq Peptide - NP_001308238
swissprot - D6R9C2
swissprot - F8WBL7
swissprot - Q15746
Ensembl - ENSG00000065534
  
Related genetic diseases (OMIM): 613780 - Aortic aneurysm, familial thoracic 7, 613780
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
 mylkaENSDARG00000034801Danio rerio
 mylkbENSDARG00000004753Danio rerio
 MYLKENSGALG00000011708Gallus gallus
 MylkENSMUSG00000022836Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
SPEG / Q15772 / SPEG complex locusENSG0000007219520
MYLK3 / Q32MK0 / myosin light chain kinase 3ENSG0000014079513
MYLK2 / Q9H1R3 / myosin light chain kinase 2ENSG0000010130612
MYLK4 / Q86YV6 / myosin light chain kinase family member 4ENSG000001459499
DAPK1 / P53355 / death associated protein kinase 1ENSG000001967309
DAPK3 / O43293 / death associated protein kinase 3ENSG000001676578
DAPK2 / Q9UIK4 / death associated protein kinase 2ENSG000000356647
O94768 / STK17B / serine/threonine kinase 17bENSG000000813206
Q9UEE5 / STK17A / serine/threonine kinase 17aENSG000001645436


Protein motifs (from Interpro)
Interpro ID Name
 IPR000719  Protein kinase domain
 IPR003598  Immunoglobulin subtype 2
 IPR003599  Immunoglobulin subtype
 IPR003961  Fibronectin type III
 IPR007110  Immunoglobulin-like domain
 IPR008271  Serine/threonine-protein kinase, active site
 IPR011009  Protein kinase-like domain superfamily
 IPR013098  Immunoglobulin I-set
 IPR013783  Immunoglobulin-like fold
 IPR015725  Myosin Light Chain Kinase 1, Kinase domain
 IPR017441  Protein kinase, ATP binding site
 IPR036116  Fibronectin type III superfamily
 IPR036179  Immunoglobulin-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006468 protein phosphorylation TAS
 biological_processGO:0006936 muscle contraction TAS
 biological_processGO:0006939 smooth muscle contraction IBA
 biological_processGO:0014820 tonic smooth muscle contraction ISS
 biological_processGO:0016310 phosphorylation IEA
 biological_processGO:0030335 positive regulation of cell migration IDA
 biological_processGO:0032060 bleb assembly IMP
 biological_processGO:0051928 positive regulation of calcium ion transport IDA
 biological_processGO:0060414 aorta smooth muscle tissue morphogenesis IMP
 biological_processGO:0071476 cellular hypotonic response IDA
 biological_processGO:0090303 positive regulation of wound healing IDA
 cellular_componentGO:0001725 stress fiber IDA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0005886 plasma membrane IDA
 cellular_componentGO:0015629 actin cytoskeleton IDA
 cellular_componentGO:0030027 lamellipodium IEA
 cellular_componentGO:0032154 cleavage furrow IEA
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0003779 actin binding IEA
 molecular_functionGO:0004672 protein kinase activity IEA
 molecular_functionGO:0004674 protein serine/threonine kinase activity IEA
 molecular_functionGO:0004687 myosin light chain kinase activity TAS
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005516 calmodulin binding IEA
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0016301 kinase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
Smooth Muscle Contraction
RHO GTPases activate PAKs


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000003 Multicystic kidney "Multicystic dysplasia of the kidney is characterized by multiple cysts of varying size in the kidney and the absence of a normal pelvocaliceal system. The condition is associated with ureteral or ureteropelvic atresia, and the affected kidney is nonfunctional." [HPO:curators]
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 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:0000021 Lower urinary tract dilatation 
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 HP:0000023 Inguinal hernia 
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 HP:0000028 Cryptorchidism "Absence of one or both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis." [HPO:curators]
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 HP:0000072 Hydroureter "The distention of the ureter with urine." [HPO:curators]
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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:0001522 Death in infancy 
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 HP:0001537 Umbilical hernia "Protrusion of abdominal contents through a defect in the abdominal wall musculature around the umbilicus. Skin and subcutaneous tissue overlie the defect." [HPO:curators]
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 HP:0001539 Omphalocele 
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 HP:0001561 Polyhydramnios 
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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:0002017 Nausea and vomiting 
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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:0002566 Intestinal malrotation "An abnormality of the intestinal rotation and fixation that normally occurs during the development of the gut. This can lead to volvulus, or twisting of the intestine that causes obstruction and necrosis." [HPO:curators]
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 HP:0002616 Aortic root dilatation 
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 HP:0002647 Aortic dissection "Aortic dissection refers to a tear in the intimal layer of the aorta causing a separation between the intima and the medial layers of the aorta." [HPO:curators]
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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:0003270 Abdominal distention "Enlargement or distention of the abdomen, which can be a secondary feature associated with a number of conditions such as bowel obstruction." [HPO:curators]
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 HP:0004388 Microcolon 
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 HP:0004933 ascending aortic dissection 
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 HP:0004942 Aortic aneurysms 
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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: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:0012763 Paroxysmal dyspnea "A sudden attack of dyspnea that occurs while the affected person is at rest." [HPO:probinson]
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 HP:0100544 Cardiac neoplasm "A `neoplasm` (MPATH:218) of the `heart` (FMA:7088)." [HPO:probinson]
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 HP:0100749 Chest pain 
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 HP:0100771 Hypoperistalsis 
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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:0100806 Sepsis 
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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
 ENSG00000180370 PAK2 / Q13177 / p21 (RAC1) activated kinase 2  / reaction
 ENSG00000101335 MYL9 / P24844 / myosin light chain 9  / reaction
 ENSG00000105357 MYH14 / Q7Z406 / myosin heavy chain 14  / reaction
 ENSG00000133026 MYH10 / P35580 / myosin heavy chain 10  / reaction
 ENSG00000092841 MYL6 / P60660 / myosin light chain 6  / reaction
 ENSG00000100345 MYH9 / P35579 / myosin heavy chain 9  / reaction
 ENSG00000118680 MYL12B / O14950 / myosin light chain 12B  / reaction
 ENSG00000133392 MYH11 / P35749 / myosin heavy chain 11  / reaction
 ENSG00000198668 CALM1 / P0DP23 / calmodulin 1  / complex / reaction






 

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