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Fgfrl1tm1.1Ptew
Targeted Allele Detail
Nomenclature
Symbol: Fgfrl1tm1.1Ptew
Name: fibroblast growth factor receptor-like 1; targeted mutation 1.1, Pascal te Welscher
MGI ID: MGI:3849002
Gene: Fgfrl1  Location: Chr5:108694229-108706950 bp, + strand  Genetic Position: Chr5, 53.24 cM, cytoband E3-F
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:149673
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129/Sv
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Fgfrl1 Mutation:  5 strains or lines available
References
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
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/15/2014
MGI 5.18
The Jackson Laboratory