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| Nomenclature |
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Symbol:
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Fgfr3tm2Wei
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Name:
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fibroblast growth factor receptor 3;
targeted mutation 2, Weizmann Institute of Science
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MGI ID: |
MGI:2135636 |
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Synonyms: |
Fgfr3G374R, FGFR3G374Rneo- |
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Gene:
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Fgfr3
Location:
Chr5:33721724-33737067 bp, + strand
Genetic Position: Chr5,
17.83 cM, cytoband B
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Anatomical defects of the Fgfr3tm2Wei/Fgfr3+ mouse
Show the 2 image(s) involving this allele.
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:54829
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Parent Cell Line:
| R1 (ES Cell) |
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Strain of Origin:
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(129X1/SvJ x 129S1/Sv)F1-Kitl+
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Mutation description |
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Allele
Type: | |
Targeted (knock-in) |
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Mutations: | |
Insertion, Single point mutation |
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Mutation details: Introduction of a G to A point mutation in codon 374 (orthologous to human codon 380) that altered the corresponding amino acid from a glycine to an arginine. A loxP flanked neomycin cassette inserted into intron 4 was removed by cre-mediated recombination. Northern blot analysis revealed that a normal molecular weight mRNA was made in homozygous mutants. (J:54829)
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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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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Fgfr3 Mutation:
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7 strains or lines available |
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| References |
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Original: |
J:54829
Wang Y et al.,
"A mouse model for achondroplasia produced by targeting fibroblast growth factor receptor 3."
Proc Natl Acad Sci U S A 1999 Apr 13;96(8):4455-60
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All: |
3 reference(s)
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