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| Nomenclature |
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Symbol:
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Fgfrl1tm1.1Ptew
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Name:
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fibroblast growth factor receptor-like 1;
targeted mutation 1.1, Pascal te Welscher
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MGI ID: |
MGI:3849002 |
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Gene:
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Fgfrl1
Location:
Chr5:108694229-108706950 bp, + strand
Genetic Position: Chr5,
53.24 cM, cytoband E3-F
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:149673
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129/Sv
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: Germ line cre mediation removed exons 3 through 7. The absence of transcript expression was confirmed by RT-PCR on E12.5 embryo extracts. (J:149673)
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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 Fgfrl1 Mutation:
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5 strains or lines available |
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| References |
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Original: |
J:149673
Catela C et al.,
"Multiple congenital malformations of Wolf-Hirschhorn syndrome are recapitulated in Fgfrl1 null mice."
Dis Model Mech 2009 May-Jun;2(5-6):283-94
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All: |
2 reference(s)
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Analysis Tools
