ENSMUSG00000020469


Mus musculus

Features
Gene ID: ENSMUSG00000020469
  
Biological name :Myl7
  
Synonyms : Myl7 / Myosin regulatory light chain 2, atrial isoform / Q9QVP4
  
Possible biological names infered from orthology : myosin light chain 7 / Q01449
  
Species: Mus musculus
  
Chr. number: 11
Strand: -1
Band: A1
Gene start: 5896637
Gene end: 5898782
  
Corresponding Affymetrix probe sets: 10384044 (MoGene1.0st)   1449071_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000099985
NCBI entrez gene - 17898     See in Manteia.
MGI - MGI:107495
RefSeq - NM_022879
RefSeq Peptide - NP_075017
swissprot - Q5SVI8
swissprot - Q9QVP4
Ensembl - ENSMUSG00000020469
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 myl7ENSDARG00000019096Danio rerio
 MYL7ENSG00000106631Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Myl2 / P51667 / Myosin regulatory light chain 2, ventricular/cardiac muscle isoform / P10916* / myosin light chain 2*ENSMUSG0000001393656
Mylpf / P97457 / Mus musculus myosin light chain, phosphorylatable, fast skeletal muscle (Mylpf), transcript variant 2, mRNA. / Q96A32* / myosin light chain, phosphorylatable, fast skeletal muscle*ENSMUSG0000003067255
Myl10 / Q62082 / Myosin regulatory light chain 10 / Q9BUA6* / myosin light chain 10*ENSMUSG0000000547453
Myl12b / Q3THE2 / Myosin regulatory light chain 12B / O14950* / myosin light chain 12B*ENSMUSG0000003486848
Myl12aENSMUSG0000002404847
Myl9 / Q9CQ19 / Myosin regulatory light polypeptide 9 ENSMUSG0000006781846


Protein motifs (from Interpro)
Interpro ID Name
 IPR002048  EF-hand domain
 IPR011992  EF-hand domain pair
 IPR018247  EF-Hand 1, calcium-binding site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 cellular_componentGO:0016459 myosin complex IEA
 cellular_componentGO:0031672 A band IEA
 cellular_componentGO:0043197 dendritic spine IDA
 molecular_functionGO:0005509 calcium ion binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
Smooth Muscle Contraction


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000269 abnormal looping morphogenesis "atypical bending of the primitive heart tube during early development" [J:27443]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0000270 abnormal heart tube morphology "malformed embryonic heart " [J:37888]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0000278 abnormal myocardial fiber morphology "malformed or poorly developed cardiac muscle fibers, the multinucleated muscle cells of the heart" [J:18048]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0000295 poorly developed ventricular trabeculae "retarded differentation of the supporting bundles of muscular fibers lining the walls of the ventricles of the heart" [J:29971]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0000297 abnormal endocardial cushion morphology "malformation of the mounds of embryonic connective tissue that bulge into the embryonic atrioventricular canal; these mounds eventually fuse to form the valves between the right and left atrioventricular orifices" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0001622 abnormal vasculogenesis "aberrant process of the initial establishment of the vascular network " [J:67296, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0001629 abnormal heart rate "greater than or fewer than average resting heart beats per minute" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0001636 irregular heartbeat "uneven timing of heart contraction" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:33038]
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Allelic Composition: Hcn2tm1Ldw/Hcn2tm1Ldw
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0001718 abnormal yolk sac "malformed extraembryonic tissue which contributes to hematopoietic circulation" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:12623]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0001719 absent vitelline blood vessels "missing vasculature of the yolk sac" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:62571, J:12623]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0001730 embryonic growth arrest "the cessation of development beyond a particular stage" [J:17509]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0001787 pericardial edema "accumulation of watery fluid in the pericardial sac of the heart" [J:52597]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0002753 dilated left ventricle "an expansion in the volume of the lower left chamber of the heart" [J:82859, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0002972 abnormal cardiac muscle contractility "altered ability of the heart muscle to shorten or to develop increased tension, often measured by dP/dT max" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Myl7tm1(cre)Krc/Myl7+,Prkg1tm2Naw/Prkg1tm2Naw
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)

 MP:0003567 abnormal cardiomyocyte proliferation "anomalous division or replication of cardiac muscle cells" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Mapk10tm1Flv/Mapk10tm1Flv,Mapk9tm1Flv/Mapk9tm1Flv
Genetic Background: B6.129S-Mapk9tm1Flv Mapk10tm1Flv

 MP:0003984 embryonic growth retardation "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0004076 abnormal vitelline vascular remodelling "anomaly in the conversion of the primary (honeycomb-like) vascular plexus of the yolk sac into a mature vascular network" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0006126 abnormal outflow tract development "anomaly in the development of the common arterial trunk that forms the aorta and pulmonary artery" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0006142 abnormal sinoatrial node conduction "anomaly in the generation or transfer of electrical impulses that trigger contraction of the atria and ventricles" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Hcn2tm1Ldw/Hcn2tm2Ldw,Myl7tm1(cre)Krc/Myl7+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0008725 enlarged heart atrium "increased size of one or both of the two upper chambers of the heart, to which the blood returns from the circulation" [MESH:A07.541.358]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0008825 abnormal cardiac epithelial to mesenchymal transition "anomaly in the process by which endocardial cells of the atrioventricular canal lose their epithelial characteristics, delaminante from the endocardial sheet, become migratory and invade the cardiac jelly, and develop mesenchymal characteristics eventaully forming the endocardial cushions reqired for septum and atrioventricular valve formation" [PMID:17303760]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0010502 ventricle myocardium hypoplasia "underdevelopment or reduced size, usually due to a reduced number of cells, of the ventricular part of the heart myocardium" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

 MP:0012253 abnormal intersomitic vessel morphology "any structural anomaly of the primary blood vessel sprouts that originate from the dorsal aorta and posterior cardinal vein and align dorsoventrally at the myotomal boundaries between somites" [MGI:anna]
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Allelic Composition: Ppargtm1Auw/Ppargtm1Auw
Genetic Background: either: 129/Sv or C57BL/6J or (involves: 129/Sv * C57BL/6J)

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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