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Rpgrip1ltm1Urt
Targeted Allele Detail
Nomenclature
Symbol: Rpgrip1ltm1Urt
Name: Rpgrip1-like; targeted mutation 1, Ulrich Ruther
MGI ID: MGI:3716208
Synonyms: Ftm-
Gene: Rpgrip1l  Location: Chr8:91217030-91313262 bp, - strand  Genetic Position: Chr8, 44.29 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:122745
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA targeted mutation was desgned to replace exons 4 and 5 with a PGK-neo cassette. The result was a truncated protein lacking all functional domains except the first coiled-coil domain. (J:122745)
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 Rpgrip1l Mutation:  17 strains or lines available
References
Original:  J:122745 Vierkotten J, et al., Ftm is a novel basal body protein of cilia involved in Shh signalling. Development. 2007 Jul;134(14):2569-77
All:  10 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
08/17/2016
MGI 6.05
The Jackson Laboratory