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| Nomenclature |
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Symbol:
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Wnt7apx-2J
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Name:
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wingless-related MMTV integration site 7A;
postaxial hemimelia 2 Jackson
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MGI ID: |
MGI:5315309 |
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Gene:
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Wnt7a
Location:
Chr6:91363981-91411363 bp, - strand
Genetic Position: Chr6,
40.45 cM
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Mutation
origin |
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Strain of Origin:
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C3HeB/FeJ or 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: A single G to T transversion in exon 4 is predicted to change amino acid residue 304 from cysteine to phenylalanine. (J:188478)
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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:188478
Harris BS et al.,
"Postaxial hemimelia 2 Jackson: a new point mutation in Wnt7a and model of Fuhrmann syndrome"
MGI Direct Data Submission 2012;():
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All: |
1 reference(s)
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Analysis Tools
