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Ift20tm1.2Gjp
Targeted Allele Detail
Summary
Symbol: Ift20tm1.2Gjp
Name: intraflagellar transport 20; targeted mutation 1.2, Gregory J Pazour
MGI ID: MGI:3817269
Synonyms: ift20null
Gene: Ift20  Location: Chr11:78427187-78432558 bp, + strand  Genetic Position: Chr11, 46.74 cM
Alliance: Ift20tm1.2Gjp page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:141071
Parent Cell Line:  AB2.2 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1b-m2
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExons 2 and 3 were removed via Cre mediated recombination of Ift20tm1.1Gjp (J:141071)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
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 Ift20 Mutation:  20 strains or lines available
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:  6 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/12/2024
MGI 6.23
The Jackson Laboratory