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| Nomenclature |
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Symbol:
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Lama2dy-7J
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Name:
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laminin, alpha 2;
dystrophia muscularis 7, Jackson
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MGI ID: |
MGI:3581452 |
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Synonyms: |
Lama2nmf417, neuroscience mutagenesis facility, 417, nmf417, NMF417 |
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Gene:
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Lama2
Location:
Chr10:26981288-27616942 bp, - strand
Genetic Position: Chr10,
14.23 cM, cytoband A4-B1
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Mutation
origin |
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Strain of Origin:
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C57BL/6J
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Mutation
description |
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Allele
Type: | |
Chemically induced (ENU) |
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Mutation: | |
Undefined |
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Mutation details: This mutation was shown by complementation analysis versus the original, dystrophia muscularis mutation to be an allele of Lama2. The molecular lesion is a single base change from T to C at the first position of codon 79, which converts Cys79 to Arg. (J:134367)
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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:82238
JAX Neuroscience Mutagenesis Facility,
"Heritable mouse mutants from JAX NMF ENU Mutagenesis Program"
MGI Direct Data Submission 2003;():
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All: |
2 reference(s)
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Analysis Tools
