ENSMUSG00000001493


Mus musculus

Features
Gene ID: ENSMUSG00000001493
  
Biological name :Meox1
  
Synonyms : Homeobox protein MOX-1 / Meox1 / P32442
  
Possible biological names infered from orthology : mesenchyme homeobox 1 / P50221
  
Species: Mus musculus
  
Chr. number: 11
Strand: -1
Band: D
Gene start: 101877510
Gene end: 101894374
  
Corresponding Affymetrix probe sets: 10391504 (MoGene1.0st)   1417595_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000051158
NCBI entrez gene - 17285     See in Manteia.
MGI - MGI:103220
RefSeq - NM_010791
RefSeq Peptide - NP_034921
swissprot - P32442
Ensembl - ENSMUSG00000001493
  

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
 MEOX1ENSG00000005102Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Meox2 / P32443 / Homeobox protein MOX-2 / P50222* / mesenchyme homeobox 2*ENSMUSG0000003614443
Gbx2 / P48031 / Homeobox protein GBX-2 / P52951* / gastrulation brain homeobox 2*ENSMUSG0000003448626
Gbx1 / P82976 / Homeobox protein GBX-1 / Q14549* / gastrulation brain homeobox 1*ENSMUSG0000006772425
Mnx1 / Q9QZW9 / motor neuron and pancreas homeobox 1 / P50219*ENSMUSG0000000156623
Nkx1-1 / NK1 transcription factor-related protein 1 / Q15270* / NK1 homeobox 1*ENSMUSG0000002911223
Evx1 / P23683 / Homeobox even-skipped homolog protein 1 / P49640* / even-skipped homeobox 1*ENSMUSG0000000550321
Nkx1-2 / P42580 / NK1 transcription factor-related protein 2 / Q9UD57* / NK1 homeobox 2*ENSMUSG0000004852821
Evx2 / P49749 / Homeobox even-skipped homolog protein 2 / Q03828* / even-skipped homeobox 2*ENSMUSG0000000181518


Protein motifs (from Interpro)
Interpro ID Name
 IPR001356  Homeobox domain
 IPR009057  Homeobox-like domain superfamily
 IPR017970  Homeobox, conserved site
 IPR020479  Homeobox domain, metazoa


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001757 somite specification IGI
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0006366 transcription by RNA polymerase II IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IGI
 biological_processGO:0060218 hematopoietic stem cell differentiation ISS
 biological_processGO:0061053 somite development IMP
 biological_processGO:0061056 sclerotome development IMP
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005737 cytoplasm IEA
 molecular_functionGO:0000978 RNA polymerase II proximal promoter sequence-specific DNA binding IDA
 molecular_functionGO:0001046 core promoter sequence-specific DNA binding IDA
 molecular_functionGO:0001077 transcriptional activator activity, RNA polymerase II proximal promoter sequence-specific DNA binding IDA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003682 chromatin binding IDA
 molecular_functionGO:0003700 DNA-binding transcription factor activity IDA
 molecular_functionGO:0043565 sequence-specific DNA binding IMP
 molecular_functionGO:0071837 HMG box domain binding IPI


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000137 abnormal vertebrae morphology "malformed bony segment of the spinal column" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1tm1Bmk/Meox1+,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000138 absent vertebrae "missing bony segments of the spinal column" [J:35802]
Show

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6

 MP:0000141 abnormal vertebral body morphology "malformed main portion of the vertebra anterior to the vertebral canal" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55583]
Show

Allelic Composition: Meox1tm1Bmk/Meox1tm1Bmk,Meox2tm1Vpa/Meox2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000151 absent rib "missing the pairs of bony structures that make up the body wall" [J:19212]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6

 MP:0000154 rib fusion "appearance of one or more ribs as a single structure" [J:62022, J:62023]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh
Genetic Background: involves: C3H/HeJ * C57BL/6

Allelic Composition: Meox1tm1Bmk/Meox1tm1Bmk,Meox2tm1Vpa/Meox2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000157 abnormal sternum morphology "malformed long flat bone of the chest; articulates with clavicle and first seven rib pairs" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:19212]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0000737 abnormal myotome development "malformation of or absence of the part of the somite that develops into the musculature" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:29279]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 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]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6

 MP:0000961 abnormal dorsal root ganglia morphology "malformed group of nerve cell bodies of each segmental nerve projecting from the spinal cord " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:60159]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0000963 fused dorsal root ganglia "loss of DRG spacing pattern and the appearance of two or more ganglia as one " [J:62022, J:62023]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0001077 abnormal spinal nerve morphology "any anomaly, deformity, or malformation of the any of the 31 paired peripheral nerves formed by the union of the dorsal and ventral spinal roots from each spinal cord segment" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0001258 decreased body length "decreased crown to tail distance compared to controls" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6

 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: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0001688 abnormal somite development "anomalous formation of any of the paired, metamerically arranged cell masses formed in the embryonic paraxial mesoderm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6

 MP:0001691 abnormal somite shape "atypical characteristic surface configuration of a segmental mass along the notochord of the developing embryo" [J:37888]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0001780 decreased brown fat amount "reduced quantity of this thermogenic form of adipose tissue" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0002114 abnormal axial skeleton morphology "abnormal development of vertebral, spinal or sternal bones resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1tm1Bmk/Meox1+,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Gt(ROSA)26Sortm1(CAG-Etv2,-GFP)Hkata/Gt(ROSA)26Sor+,Meox1tm1(cre)Jpa/Meox1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0002632 vestigial tail "a trace or rudimentary tail structure; the degenerated remains of any tail structure" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6

 MP:0002823 abnormal rib development "anomalous formation of the bones forming the bony wall of the chest" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:84754]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh
Genetic Background: involves: C3H/HeJ * C57BL/6

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

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0004206 abnormal dermomyotome development "any structural anomaly of the portion of the embryonic somite that remains after migration of the sclerotomic tissue" [J:50279, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0004248 abnormal epaxial muscle morphology "any structural anomaly of the muscles derived from the medial myotome; includes the intrinsic back muscles" [PMID:1591996]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0004609 vertebral fusion "the union of one or more vertebrae into a single structure" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh
Genetic Background: involves: C3H/HeJ * C57BL/6

 MP:0004619 caudal vertebral fusion "the union of one or more caudal vertebrae into a single structure in species where this does not normally occur" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Meox1tm1Bmk/Meox1+,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Meox1tm1Bmk/Meox1tm1Bmk,Meox2tm1Vpa/Meox2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004653 absent caudal vertebrae "absence of all of the bony segments of the coccyx or tail; there are usually 27-30 present in rodents and only 3-5 fused vertebrae in human" [MESH:National Library of Medicine_Medical Subject Headings]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0004703 abnormal vertebral column "any structural anomaly of the complete structure forming the rostral-caudal axis of the skeleton formed from the alternating segments of vertebra and intervertebral discs which support the spinal cord" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0005222 abnormal somite size "atypical size of any of the segmental masses along the notochord of the developing embryo" [J:72325]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0005223 abnormal anterior-posterior polarity of the somites "anomalous development or formation of the somites along the axis that runs from the front to the back surface of the body " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, J:72325]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0005225 abnormal vertebrae development "anomalous formation of the vertebrae from the sclerotome" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh
Genetic Background: involves: C3H/HeJ * C57BL/6

Allelic Composition: Meox1tm1Bmk/Meox1tm1Bmk,Meox2tm1Vpa/Meox2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005421 loose skin "condition in which the skin hangs in folds" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0006029 abnormal sclerotome "malformation of the one or more of the masses of mesodermal tissue that is derived from the somites and is adjacent to the notochord that give rise to the ribs and vertebrae" [smb:Susan M Bello, Mouse Genome Informatics Curator, Taber s Cyclopedic Medical Dictionary:19th edition: ISBN N 0-8036-0655-99]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0008832 hemivertebra "a congenital malformation of the spine in which only half of a vertebral body develops" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh
Genetic Background: involves: C3H/HeJ * C57BL/6

 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: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh,Meox2tm1Vpa/Meox2tm1Vpa
Genetic Background: involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6

 MP:0030286 occipital bone hypoplasia "underdevelopment or reduced size, usually due to a reduced number of cells, of the bone at the lower, posterior part of the skull" [MGI:anna]
Show

Allelic Composition: Bmi1tm1Brn/Bmi1+
Genetic Background: involves: 129P2/OlaHsd

  


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






 

1 s.

 
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