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| Nomenclature |
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Symbol:
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Agrnnmf380
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Name:
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agrin;
neuroscience mutagenesis facility, 380
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MGI ID: |
MGI:3614578 |
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Synonyms: |
NMF380 |
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Gene:
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Agrn
Location:
Chr4:156165290-156185901 bp, - strand
Genetic Position: Chr4,
88.55 cM
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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: | |
Single point mutation |
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Mutation details: This phenotypic mutation was identified in an ENU mutagenesis screen. The molecular mutation is an A to G conversion, resulting in the change of phenylalanine 1061 to serine (F1061S, numbered according to the SN form of the protein) in the SEA domain of the encoded protein. (J:176117)
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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:87349
JAX Neuroscience Mutagenesis Facility,
"Heritable mouse mutants from JAX NMF ENU Mutagenesis Program"
MGI Direct Data Submission 2004-7;():
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All: |
2 reference(s)
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Analysis Tools
