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Apctm1.1Alew
Targeted Allele Detail
Summary
Symbol: Apctm1.1Alew
Name: APC, WNT signaling pathway regulator; targeted mutation 1.1, Anabelle Lewis
MGI ID: MGI:5305725
Synonyms: APC1322T
Gene: Apc  Location: Chr18:34353977-34455605 bp, + strand  Genetic Position: Chr18, 18.53 cM
Alliance: Apctm1.1Alew page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:180275
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA floxed neo cassette replaced the sequence corresponding to amino acids 1323 to 2845 and resulted in the deletion of all but one 20AAR domain with a truncation of the produced protein at 1322 (1322T). Cre-mediated recombination removed the floxed neo cassette inserted downstream of the modified exon 15. (J:180275)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Tumor Data
List all tumor models in MMHCdb carrying Apctm1.1Alew
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 Apc Mutation:  158 strains or lines available
References
Original:  J:180275 Pollard P, et al., The Apc 1322T mouse develops severe polyposis associated with submaximal nuclear beta-catenin expression. Gastroenterology. 2009 Jun;136(7):2204-2213.e1-13
All:  9 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
11/19/2024
MGI 6.24
The Jackson Laboratory