ENSMUSG00000020381


Mus musculus

Features
Gene ID: ENSMUSG00000020381
  
Biological name :Mrnip
  
Synonyms : MRN complex-interacting protein / Mrnip / Q9D1F5
  
Possible biological names infered from orthology : Q6NTE8
  
Species: Mus musculus
  
Chr. number: 11
Strand: 1
Band: B1.3
Gene start: 50174444
Gene end: 50200115
  
Corresponding Affymetrix probe sets: 10375704 (MoGene1.0st)   1446800_at (Mouse Genome 430 2.0 Array)   1448930_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000020647
Ensembl peptide - ENSMUSP00000115263
NCBI entrez gene - 68067     See in Manteia.
MGI - MGI:1915317
RefSeq - NM_026543
RefSeq Peptide - NP_080819
swissprot - F6S5X0
swissprot - Q9D1F5
Ensembl - ENSMUSG00000020381
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 mrnipENSDARG00000074071Danio rerio
 MRNIPENSGALG00000035476Gallus gallus
 MRNIPENSG00000161010Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR032739  MRN complex-interacting protein


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006281 DNA repair IEA
 biological_processGO:0006974 cellular response to DNA damage stimulus ISO
 biological_processGO:0007095 mitotic G2 DNA damage checkpoint IEA
 biological_processGO:0008150 biological_process ND
 biological_processGO:0010212 response to ionizing radiation IEA
 biological_processGO:0045860 positive regulation of protein kinase activity IEA
 biological_processGO:0071168 protein localization to chromatin IEA
 biological_processGO:1905168 positive regulation of double-strand break repair via homologous recombination IEA
 biological_processGO:2001032 regulation of double-strand break repair via nonhomologous end joining IEA
 cellular_componentGO:0005575 cellular_component ND
 cellular_componentGO:0005634 nucleus ISO
 cellular_componentGO:0005654 nucleoplasm ISS
 cellular_componentGO:0030870 Mre11 complex IEA
 molecular_functionGO:0003674 molecular_function ND
 molecular_functionGO:0003682 chromatin binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001399 hyperactivity "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125]
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Allelic Composition: Magel2tm1Stw/Magel2tm1Stw
Genetic Background: C57BL/6-Magel2tm1Stw/J

  


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






 

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