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Search results 701 to 729 out of 729 for Meox1

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Type Details Score
Publication
- | J:63103
     
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
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Publication
- | J:155721
     
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
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Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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Publication
- | J:262123
     
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
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Publication
- | J:91388
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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DO Term
DOID:0080590 | Klippel-Feil syndrome 2
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Allele
Meox1<em1(dre)Smoc> | MGI:6724282
Name: mesenchyme homeobox 1; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Recombinase
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Allele
Meox1<squig> | MGI:5780171
Name: mesenchyme homeobox 1; squiggle tail
Allele Type: Spontaneous
Attribute String: Null/knockout
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Strain
MGI:6429170 | C57BL/6J-Meox1<em1(dre)Smoc>/Smoc
Attribute String: coisogenic, mutant strain, endonuclease-mediated mutation
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Publication
23290072 | -
First Author: Mohamed JY
Year: 2013
Journal: Am J Hum Genet
Title: Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.
Volume: 92
Issue: 1
Pages: 157-61
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Protein Domain
IPR042634 | MOX-1/MOX-2
Type: Family
Description: MEOX1 and MEOX2 are homeodomain transcription factors that have been shown to be partially functionally redundant during development. They regulate the cyclin dependent kinase inhibitors p21 and p16 in vascular endothelial cells []. Nevertheless, MEOX1 also plays important, non-redundant roles in maintaining sclerotome polarity and the formation of cranio-cervical joints []. Mutations in the MEOX1 gene cause Klippel-Feil syndrome 2, autosomal recessive (KFS2), a skeletal disorder characterised by congenital fusion of cervical vertebrae [, ].
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Allele
Meox1<em2Smoc> | MGI:7291030
Name: mesenchyme homeobox 1; endonuclease-mediated mutation 2, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Conditional ready, No functional change
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Strain
MGI:7623430 | C57BL/6J-Meox1<em2Smoc>/Smoc
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
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Strain
MGI:5780172 | BALB/cJ-Meox1<squig>/GrsrJ
Attribute String: spontaneous mutation, mutant strain, coisogenic
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Genotype
Genotype
Symbol: Meox1/Meox1
Background: BALB/cJ-Meox1/GrsrJ
Zygosity: hm
Has Mutant Allele: true
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Allele
Tg(Meox1-TagRFP/cre/ERT2)30Amc | MGI:5435690
Name: transgene insertion 30, Andrew P McMahon
Allele Type: Transgenic
Attribute String: Inducible, Recombinase, Reporter
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Strain
MGI:5435694 | B6;D-Tg(Meox1-TagRFP/cre/ERT2)30Amc/J
Attribute String: mutant stock, transgenic
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Publication
- | J:187214
     
First Author: McMahon AP
Year: 2012
Journal: MGI Direct Data Submission
Title: Generation of a Meox1-TagRFP/cre/ERT2 transgene
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Allele
Tg(RP11-209M4*)#Gglo | MGI:5304447
Name: transgene insertion, Gabriela G Loots
Allele Type: Transgenic
Attribute String: Inserted expressed sequence
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Strain
MGI:5304680 | FVB-Tg(RP11-209M4*)#Gglo
Attribute String: transgenic, mutant strain, coisogenic
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Genotype
Genotype
Symbol: Tg(RP11-209M4*)#Gglo/?
Background: FVB-Tg(RP11-209M4*)#Gglo
Zygosity: ot
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Tg(RP11-209M4*)#Gglo/Tg(RP11-209M4*)#Gglo
Background: FVB-Tg(RP11-209M4*)#Gglo
Zygosity: hm
Has Mutant Allele: true
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Publication
29217079 | J:274119
First Author: Combes AN
Year: 2018
Journal: Kidney Int
Title: Haploinsufficiency for the Six2 gene increases nephron progenitor proliferation promoting branching and nephron number.
Volume: 93
Issue: 3
Pages: 589-598
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Publication
15965026 | J:99965
First Author: Loots GG
Year: 2005
Journal: Genome Res
Title: Genomic deletion of a long-range bone enhancer misregulates sclerostin in Van Buchem disease.
Volume: 15
Issue: 7
Pages: 928-35
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Protein
P32442
Organism: Mus musculus/domesticus
Length: 253  
Fragment?: false
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Protein
P32443
Organism: Mus musculus/domesticus
Length: 303  
Fragment?: false
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Protein
Q99M23
Organism: Mus musculus/domesticus
Length: 303  
Fragment?: false
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Protein
Q3UZS8
Organism: Mus musculus/domesticus
Length: 159  
Fragment?: true
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Publication
- | J:159099
     
First Author: McMahon A
Year: 2010
Journal: Unpublished
Title: Summary of mouse strains characterized by GUDMAP consortium.
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