|
|
| Nomenclature |
|
Symbol:
|
Ift20tm1.1Gjp
|
|
Name:
|
intraflagellar transport 20;
targeted mutation 1.1, Gregory J Pazour
|
|
MGI ID: |
MGI:3817268 |
|
Synonyms: |
ift20flox |
|
Gene:
|
Ift20
Location:
Chr11:78536361-78541737 bp, + strand
Genetic Position: Chr11,
46.74 cM
|
|
Mutation
origin |
|
Germline Transmission:
|
Earliest citation of germline transmission:
J:141071
|
|
Parent Cell Line:
| AB2.2 (ES Cell) |
|
Strain of Origin:
|
129S7/SvEvBrd-Hprtb-m2
|
|
Mutation
description |
|
Allele
Type: | |
Targeted (Floxed/Frt) |
|
Mutation: | |
Insertion |
| |
|
Mutation details: An frt flanked neo cassette followed by a loxP site were inserted into intron 1 and a second loxP site was inserted into intron 3 via homologous recombination. The neo cassette was then removed via in vivo Flp mediated recombination. (J:141071)
|
|
Phenotypes
|
View phenotypes for all genotypes (concatenated display).
|
| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
|
| References |
|
Original: |
J:141071
Jonassen JA et al.,
"Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease."
J Cell Biol 2008 Nov 3;183(3):377-84
|
|
All: |
4 reference(s)
|
|
Analysis Tools
