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| Nomenclature |
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Symbol:
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Msx2tm1Rilm
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Name:
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homeobox, msh-like 2;
targeted mutation 1, Richard Maas
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MGI ID: |
MGI:1926381 |
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Synonyms: |
Msx2- |
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Gene:
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Msx2
Location:
Chr13:53466881-53473074 bp, - strand
Genetic Position: Chr13,
27.84 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:61509
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Parent Cell Line:
| J1 (ES Cell) |
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Strain of Origin:
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129S4/SvJae
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutation: | |
Insertion |
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Mutation details: Gene disruption caused by insertion of a pMC1-neo cassette into coding sequences located just 5' to the homeobox domain in exon 2. (J:61509)
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Inheritance: | |
Recessive |
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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Original: |
J:61509
Satokata I et al.,
"Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation."
Nat Genet 2000 Apr;24(4):391-5
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All: |
26 reference(s)
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Analysis Tools
