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| Nomenclature |
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Symbol:
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Lamc3tm1.1Wjbr
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Name:
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laminin gamma 3;
targeted mutation 1.1, William J Brunken
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MGI ID: |
MGI:4941480 |
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Synonyms: |
Lamc3tm1Wjbr |
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Gene:
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Lamc3
Location:
Chr2:31887291-31946539 bp, + strand
Genetic Position: Chr2,
21.93 cM, cytoband B
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:169656
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129X1/SvJ
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Mutation
description |
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Allele
Type: | |
Targeted (Reporter) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: A 2.2 kb fragment spanning exon 1 and part of intron 1 was replaced with an IRES betageo cassette via homologous recombination. The neo selection cassette was removed by mating the heterozygous mouse with a sperm-Cre expressing mouse. (J:169656, J:184380)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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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 Lamc3 Mutation:
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3 strains or lines available |
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| References |
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Original: |
J:169656
Denes V et al.,
"Laminin deficits induce alterations in the development of dopaminergic neurons in the mouse retina."
Vis Neurosci 2007 Jul-Aug;24(4):549-62
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All: |
4 reference(s)
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Analysis Tools
