ENSMUSG00000018143


Mus musculus

Features
Gene ID: ENSMUSG00000018143
  
Biological name :Mafk
  
Synonyms : Mafk / Q61827 / v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian)
  
Possible biological names infered from orthology : MAF bZIP transcription factor K / O60675
  
Species: Mus musculus
  
Chr. number: 5
Strand: 1
Band: G2
Gene start: 139791513
Gene end: 139802653
  
Corresponding Affymetrix probe sets: 10526961 (MoGene1.0st)   1418616_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000018287
Ensembl peptide - ENSMUSP00000106460
NCBI entrez gene - 17135     See in Manteia.
MGI - MGI:99951
RefSeq - XM_006504653
RefSeq - NM_010757
RefSeq Peptide - NP_034887
swissprot - Q3UP84
swissprot - Q61827
Ensembl - ENSMUSG00000018143
  

This gene has been taged as a transcription factor by TFT
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 mafkENSDARG00000100947Danio rerio
 MAFKENSGALG00000004189Gallus gallus
 MAFKENSG00000198517Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Mafg / O54790 / Transcription factor MafG / O15525* / MAF bZIP transcription factor G*ENSMUSG0000005151074
Maff / O54791 / Transcription factor MafF / Q9ULX9* / MAF bZIP transcription factor F*ENSMUSG0000004262265
Mafb / P54841 / Transcription factor MafB / Q9Y5Q3* / MAF bZIP transcription factor B*ENSMUSG0000007462247
Maf / P54843 / Transcription factor Maf / O75444* / MAF bZIP transcription factor*ENSMUSG0000005543543
Mafa / Q8CF90 / Transcription factor MafA / Q8NHW3* / MAF bZIP transcription factor A*ENSMUSG0000004759142
Nrl / P54846 / Neural retina-specific leucine zipper protein / P54845* / neural retina leucine zipper*ENSMUSG0000004063235


Protein motifs (from Interpro)
Interpro ID Name
 IPR004826  Basic leucine zipper domain, Maf-type
 IPR004827  Basic-leucine zipper domain
 IPR008917  Transcription factor, Skn-1-like, DNA-binding domain superfamily
 IPR024874  Transcription factor Maf family
 IPR028574  Transcription factor MafK


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000122 negative regulation of transcription by RNA polymerase II IEA
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IDA
 biological_processGO:0007399 nervous system development IEA
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0005654 nucleoplasm IEA
 molecular_functionGO:0000976 transcription regulatory region sequence-specific DNA binding IEA
 molecular_functionGO:0001221 transcription cofactor binding IEA
 molecular_functionGO:0003677 DNA binding IDA
 molecular_functionGO:0003700 DNA-binding transcription factor activity IDA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0043565 sequence-specific DNA binding IEA
 molecular_functionGO:0071535 RING-like zinc finger domain binding IEA


Pathways (from Reactome)
Pathway description
Factors involved in megakaryocyte development and platelet production


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000229 abnormal megakaryocyte differentiation "atypical process of formation and development these very large bone marrow cells which release mature platelets" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafk+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0000240 extramedullary hematopoiesis "formation and development of blood cells outside the bone marrow, e.g., in the spleen, liver, or lymph nodes" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0000243 myoclonus "involuntary shock-like contractions, variable in rhythm and amplitude, followed by relaxation, of a muscle or a group of muscles; generally due to a central nervous system lesion" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafk+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0000691 enlarged spleen "increased spleen size" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0001393 ataxia "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0001402 hypoactivity "reduced movement from one place to another" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:64289]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafk+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0001513 limb grasping "mice clasp front and/or hind feet almost immediately upon being lifted by tail" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafk+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0001577 anemia "less than normal levels of red blood cells, hemoglobin or volume of packed red blood cells " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:53370]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0002447 abnormal erythrocyte morphology "structural anomaly of the cells in the blood that carry oxygen, red blood cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0002640 reticulocytosis "an increase in the number of reticulocytes in the blood" [J:78271, cwg:Carroll W. Goldsmith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0002882 abnormal neuron "anomaly in the functional cells of the nervous system that receive, conduct, and transmit impulses " [MeSH:National Library of Medicine - Medical Subject Headings, 2003]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafk+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0003179 decreased platelet count "fewer than the normal numbers of the non-nucleated cells found in the blood and involved in blood coagulation " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, hdene:Howard Dene , Mouse Genome Informatics Curator, J:93052]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafk+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0003657 abnormal erythrocyte lysis "increase or decrease in the ability of RBCs to withstand changes in osmolarity" [smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0011090 partial perinatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith]
Show

Allelic Composition: Mafgtm1Jeng/Mafgtm1Jeng,Mafktm1Jeng/Mafktm1Jeng
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

  


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






 

1 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr