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Ift172tm1Lmgd
Targeted Allele Detail
Summary
Symbol: Ift172tm1Lmgd
Name: intraflagellar transport 172; targeted mutation 1, Laboratory of Mammalian Genes and Development, Heiner Westphal
MGI ID: MGI:3829198
Synonyms: Slb
Gene: Ift172  Location: Chr5:31410623-31448458 bp, - strand  Genetic Position: Chr5, 17.27 cM, cytoband B1
Alliance: Ift172tm1Lmgd page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:143572
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 detailsThe first 3 exons were replaced with a neo cassette via homologous recombination. RT-PCR analysis detects the presence of a truncated mRNA fragment corresponding to the 3' non-deleted region in mutants. (J:143572)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 8 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 Ift172 Mutation:  75 strains or lines available
References
Original:  J:143572 Gorivodsky M, et al., Intraflagellar transport protein 172 is essential for primary cilia formation and plays a vital role in patterning the mammalian brain. Dev Biol. 2009 Jan 1;325(1):24-32
All:  1 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
04/09/2024
MGI 6.23
The Jackson Laboratory