ENSMUSG00000028312


Mus musculus

Features
Gene ID: ENSMUSG00000028312
  
Biological name :Smc2
  
Synonyms : Q8CG48 / Smc2 / Structural maintenance of chromosomes protein 2
  
Possible biological names infered from orthology : O95347 / structural maintenance of chromosomes 2
  
Species: Mus musculus
  
Chr. number: 4
Strand: 1
Band: B2
Gene start: 52439243
Gene end: 52488260
  
Corresponding Affymetrix probe sets: 10504957 (MoGene1.0st)   1429658_a_at (Mouse Genome 430 2.0 Array)   1429659_at (Mouse Genome 430 2.0 Array)   1429660_s_at (Mouse Genome 430 2.0 Array)   1448635_at (Mouse Genome 430 2.0 Array)   1458479_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000114228
Ensembl peptide - ENSMUSP00000099979
Ensembl peptide - ENSMUSP00000113940
NCBI entrez gene - 14211     See in Manteia.
MGI - MGI:106067
RefSeq - NM_001301412
RefSeq - NM_008017
RefSeq Peptide - NP_001288341
RefSeq Peptide - NP_032043
swissprot - B1AWH6
swissprot - Q8CG48
Ensembl - ENSMUSG00000028312
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 smc2ENSDARG00000017744Danio rerio
 SMC2ENSGALG00000015691Gallus gallus
 SMC2ENSG00000136824Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR003395  RecF/RecN/SMC, N-terminal
 IPR010935  SMCs flexible hinge
 IPR024704  Structural maintenance of chromosomes protein
 IPR027120  Smc2, ATP-binding cassette domain
 IPR027417  P-loop containing nucleoside triphosphate hydrolase
 IPR036277  SMCs flexible hinge superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007049 cell cycle IEA
 biological_processGO:0007076 mitotic chromosome condensation ISO
 biological_processGO:0010032 meiotic chromosome condensation IMP
 biological_processGO:0030261 chromosome condensation IEA
 biological_processGO:0045132 meiotic chromosome segregation IMP
 biological_processGO:0051276 chromosome organization IEA
 biological_processGO:0051301 cell division IEA
 biological_processGO:0051383 kinetochore organization IMP
 cellular_componentGO:0000228 nuclear chromosome ISO
 cellular_componentGO:0000793 condensed chromosome ISO
 cellular_componentGO:0000796 condensin complex ISO
 cellular_componentGO:0005634 nucleus ISO
 cellular_componentGO:0005694 chromosome IEA
 cellular_componentGO:0005730 nucleolus ISO
 cellular_componentGO:0005737 cytoplasm IEA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0046982 protein heterodimerization activity ISO


Pathways (from Reactome)
Pathway description
Condensation of Prophase Chromosomes
Condensation of Prometaphase Chromosomes


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000788 abnormal cerebral cortex morphology "malformed gray cellular mantle covering the surface of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:38857]
Show

Allelic Composition: Ncaphtm1.1Itl/Ncaphtm1.2Itl,Ncaph2tm1.1Itl/Ncaph2tm1.2Itl,Tg(Nes-cre)1Kln/0
Genetic Background: involves: C57BL/6 * C57BL/6J * SJL

 MP:0003111 abnormal nucleus morphology "abnormalities in the nucleus and/or its surrounding membrane" [J:91473, smb:Susan M. Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Ncaphtm1.1Itl/Ncaphtm1.2Itl,Ncaph2tm1.1Itl/Ncaph2tm1.2Itl,Tg(Nes-cre)1Kln/0
Genetic Background: involves: C57BL/6 * C57BL/6J * SJL

 MP:0004046 abnormal mitosis "anomaly in the process of cell division including both division of the nucleus (karyokinesis) and the cytoplasm (cytokinesis) " [smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Ncaphtm1.1Itl/Ncaphtm1.2Itl,Ncaph2tm1.1Itl/Ncaph2tm1.2Itl,Tg(Nes-cre)1Kln/0
Genetic Background: involves: C57BL/6 * C57BL/6J * SJL

 MP:0006254 thin cerebral cortex "decreased depth of the mantle covering the surface of the cerebral hemispheres" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:84683]
Show

Allelic Composition: Ncaphtm1.1Itl/Ncaphtm1.2Itl,Ncaph2tm1.1Itl/Ncaph2tm1.2Itl,Tg(Nes-cre)1Kln/0
Genetic Background: involves: C57BL/6 * C57BL/6J * SJL

 MP:0008948 decreased neuron number "fewer than normal numbers of the cells of the nervous system that receive, conduct, and transmit impulses" [MESH:A08.663]
Show

Allelic Composition: Ncaphtm1.1Itl/Ncaphtm1.2Itl,Ncaph2tm1.1Itl/Ncaph2tm1.2Itl,Tg(Nes-cre)1Kln/0
Genetic Background: involves: C57BL/6 * C57BL/6J * SJL

 MP:0011092 complete embryonic lethality "death of all organisms of a given genotype in a population within the embryonic period prior to organogenesis (Mus: prior to E14)" [MGI:csmith]
Show

Allelic Composition: Mcph1Tg(HLA-A2.1)1Enge/Mcph1+
Genetic Background: NOD.B6-Mcph1Tg(HLA-A2.1)1Enge

 MP:0012203 abnormal neuronal stem cell morphology "any structural anomaly of an undifferentiated cell that originates from the neuroectoderm and has the capacity both to perpetually self-renew without differentiating and to generate multiple types of lineage-restricted progenitors" [CL:0000047]
Show

Allelic Composition: Ncaphtm1.1Itl/Ncaphtm1.2Itl,Ncaph2tm1.1Itl/Ncaph2tm1.2Itl,Tg(Nes-cre)1Kln/0
Genetic Background: involves: C57BL/6 * C57BL/6J * SJL

 MP:0012204 abnormal neuronal stem cell physiology "any functional anomaly of an undifferentiated cell that originates from the neuroectoderm and has the capacity both to perpetually self-renew without differentiating and to generate multiple types of lineage-restricted progenitors" [CL:0000047]
Show

Allelic Composition: Ncaphtm1.1Itl/Ncaphtm1.2Itl,Ncaph2tm1.1Itl/Ncaph2tm1.2Itl,Tg(Nes-cre)1Kln/0
Genetic Background: involves: C57BL/6 * C57BL/6J * SJL

  


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






 

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