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Ctnna1del
Spontaneous Allele Detail
Summary
Symbol: Ctnna1del
Name: catenin alpha 1; deletion
MGI ID: MGI:3764945
Synonyms: Ctnna1del
Gene: Ctnna1  Location: Chr18:35251955-35387829 bp, + strand  Genetic Position: Chr18, 18.89 cM
Alliance: Ctnna1del page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:127452
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Spontaneous (Hypomorph)
Mutation:    Intragenic deletion
 
Mutation detailsA 4107 bp deletion encompassing exons 3 and 4 occurred in the locus, leading to a frameshift mutation at codon 101. Expression levels of the mutant allele are reduced by two-thirds as measured by RT-PCR analysis, and the protein generated is predicted to not be able to interact with its heterodimer partners. (J:127452)
Inheritance:    Other (see notes)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Ctnna1 Mutation:  133 strains or lines available
Notes
This mutation arose on a APCtm1.1Tno background and leads to a reversion of the tumorogenesis phenotype associated with the APC allele. This reversion only occurs when the two mutant alleles are in cis-configuration.
References
Original:  J:127452 Shibata H, et al., Alpha-catenin is essential in intestinal adenoma formation. Proc Natl Acad Sci U S A. 2007 Nov 13;104(46):18199-204
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
04/23/2024
MGI 6.23
The Jackson Laboratory