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| Nomenclature |
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Symbol:
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Msx1tm1Bero
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Name:
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homeobox, msh-like 1;
targeted mutation 1, Benoit Robert
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MGI ID: |
MGI:1933766 |
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Synonyms: |
Msx1-, Msx1nlacZ, Msx1-nlacZ |
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Gene:
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Msx1
Location:
Chr5:37820485-37824583 bp, - strand
Genetic Position: Chr5,
20.21 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:42035
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Parent Cell Line:
| HM-1 (ES Cell) |
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Strain of Origin:
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129P2/OlaHsd-Hprtb-m3
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Mutation
description |
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Allele
Type: | |
Targeted (Reporter) |
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Mutation: | |
Insertion |
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Mutation details: An n-lacZ reporter gene was inserted in-frame into the sequence encoding the third helix of the homeodomain. A fusion protein of the first 43 amino acids and beta-galactosidase is expressed from this allele. (J:42035)
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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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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Msx1 Mutation:
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5 strains or lines available |
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| References |
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Original: |
J:42035
Houzelstein D et al.,
"Insertional mutation of the mouse Msx1 homeobox gene by an nlacZ reporter gene."
Mech Dev 1997 Jul;65(1-2):123-33
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All: |
24 reference(s)
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Analysis Tools
