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Apctm2.1Alew
Targeted Allele Detail
Summary
Symbol: Apctm2.1Alew
Name: APC, WNT signaling pathway regulator; targeted mutation 1.1, Anabelle Lewis
MGI ID: MGI:5305728
Synonyms: APCdeltaSAMP
Gene: Apc  Location: Chr18:34353977-34455605 bp, + strand  Genetic Position: Chr18, 18.53 cM
Alliance: Apctm2.1Alew page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:180057
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 15 was replaced with a modified one in which sequence corresponding to amino acids 1322 to 2006 was deleted. This deletion corresponds to the SAMP repeats. Cre-mediated recombination removed the neo cassette inserted downstream of the modified exon 15. (J:180057)
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 Apctm2.1Alew
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:  154 strains or lines available
References
Original:  J:180057 Lewis A, et al., The C-terminus of Apc does not influence intestinal adenoma development or progression. J Pathol. 2012 Jan;226(1):73-83
All:  2 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