ENSMUSG00000079471


Mus musculus

Features
Gene ID: ENSMUSG00000079471
  
Biological name :Mymx
  
Synonyms : Mymx / Protein myomixer / Q2Q5T5
  
Possible biological names infered from orthology : A0A1B0GTQ4 / myomixer, myoblast fusion factor
  
Species: Mus musculus
  
Chr. number: 17
Strand: -1
Band: B3
Gene start: 45600971
Gene end: 45602102
  
Corresponding Affymetrix probe sets: 10451142 (MoGene1.0st)   1456242_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000109157
Ensembl peptide - ENSMUSP00000126690
Ensembl peptide - ENSMUSP00000137630
Ensembl peptide - ENSMUSP00000146823
NCBI entrez gene - 653016     See in Manteia.
MGI - MGI:3649059
RefSeq - XM_006524790
RefSeq - NM_001177468
RefSeq - NM_001177469
RefSeq - NM_001177470
RefSeq - XM_006524789
RefSeq Peptide - NP_001170940
RefSeq Peptide - NP_001170941
RefSeq Peptide - NP_001170939
swissprot - Q2Q5T5
swissprot - A0A223PZC0
Ensembl - ENSMUSG00000079471
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 MYMXENSG00000262179Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
No match


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007517 muscle organ development IEA
 biological_processGO:0007520 myoblast fusion IMP
 biological_processGO:0045026 plasma membrane fusion IDA
 biological_processGO:0060538 skeletal muscle organ development IMP
 cellular_componentGO:0000139 Golgi membrane IDA
 cellular_componentGO:0005789 endoplasmic reticulum membrane IDA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000747 muscle weakness "loss of muscle strength" [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0000759 abnormal skeletal muscle morphology "anomalous structure of any of the striated muscle fibers connected at either or both extremeties with the bony framework of the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0001575 cyanosis "a dark bluish or purple skin discoloration resulting from deficient oxygenation of the blood" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60159]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0002108 abnormal muscle morphology "abnormal development of muscle tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0002109 abnormal limb morphology "abnormal development of limbs resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0002280 abnormal intercostal muscle morphology "anomaly in the respiratory muscles that arise from the lower border of one rib and insert into the upper border of the adjoining rib " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0003358 abnormal hypaxial muscle morphology "malformation of the muscles of the limbs" [smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0004174 abnormal spine curvature "deviation from the typical S-shape of the spine" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0009431 decreased fetal weight "reduced weight of a fetus compared to controls (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0010819 primary atelectasis "nonexpansion of the lungs after birth, seen in stillborn organisms and in live born animals that do not establish respiration" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0011087 complete neonatal lethality "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

Allelic Composition: Mymxem2Shcs/Mymxem2Shcs
Genetic Background: involves: C57BL/6J

 MP:0011808 abnormal myoblast differentiation "anomaly in the process in which a relatively unspecialized cell acquires specialized features of a myoblast, a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into striated muscle fibers" [GO:0045445]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

 MP:0012269 nuchal edema "abnormal accumulation of subcutaneous fluid in the nuchal region i.e. at the back of the neck" [MGI:anna]
Show

Allelic Composition: Cxcr5tm1.1Namt/Cxcr5tm1.1Namt,Tg(Itgax-cre)1-1Reiz/0,Tg(Prnp)a20Cwe/0
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA

  


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






 

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