Ift20^tm1.2Gjp
Targeted Allele Detail

Summary

• Symbol: Ift20^tm1.2Gjp
• Name: intraflagellar transport 20; targeted mutation 1.2, Gregory J Pazour
• MGI ID: MGI:3817269
• Synonyms: ift20^null
• Gene: Ift20 Location: Chr11:78427187-78432558 bp, + strand Genetic Position: Chr11, 46.74 cM
• Alliance: Ift20^tm1.2Gjp page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:141071
• Parent Cell Line: AB2.2 (ES Cell)
• Strain of Origin: 129S7/SvEvBrd-Hprt1^b-m2

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion
• Mutation details: Exons 2 and 3 were removed via Cre mediated recombination of Ift20^tm1.1Gjp (J:141071)

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: 21 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)