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| Nomenclature |
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Symbol:
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Fras1bl
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Name:
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Fraser syndrome 1 homolog (human);
blebbed
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MGI ID: |
MGI:1856691 |
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Gene:
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Fras1
Location:
Chr5:96373955-96784728 bp, + strand
Genetic Position: Chr5,
47.29 cM
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Mutation
origin |
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Strain of Origin:
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(C3H/HeH x 101/H)F1
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Mutation
description |
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Allele
Type: | |
Radiation induced |
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Mutation: | |
Nucleotide substitutions |
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Mutation details: The mutation in the blebbed mouse was identified as nucleotide changes within the 47th exon. This nonsense mutation 7313CC to AA (S2200X) was not identified in 9 other strains of mice. (J:83745)
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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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Analysis Tools
