About   Help   FAQ
Ift122sopb
Chemically induced Allele Detail
Summary
Symbol: Ift122sopb
Name: intraflagellar transport 122; sister of open brain
MGI ID: MGI:3578529
Gene: Ift122  Location: Chr6:115830431-115903660 bp, + strand  Genetic Position: Chr6, 53.72 cM
Alliance: Ift122sopb page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU) (Null/knockout)
Mutation:    Single point mutation
 
Mutation detailsENU treatment induced a T-to-C transition mutation in the start codon (p.M1T). Western blot analysis confirms the absence of protein in homozygous embryos at E12.5 and E13.5. (J:168317)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 10 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 Ift122 Mutation:  52 strains or lines available
References
Original:  J:98216 Garcia-Garcia MJ, et al., Inaugural Article: Analysis of mouse embryonic patterning and morphogenesis by forward genetics. Proc Natl Acad Sci U S A. 2005 Apr 26;102(17):5913-9
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/19/2024
MGI 6.23
The Jackson Laboratory