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Apptm2.1Ldad
Targeted Allele Detail
Summary
Symbol: Apptm2.1Ldad
Name: amyloid beta precursor protein; targeted mutation 2.1, Luciano D'Adamio
MGI ID: MGI:4868765
Synonyms: AppY682G, APP YG
Gene: App  Location: Chr16:84751236-84972187 bp, - strand  Genetic Position: Chr16, 46.92 cM, cytoband C3-qter
Alliance: Apptm2.1Ldad page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:166989
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsExon 16 was replaced with a floxed neo cassette and a modified exon 16 in which a point mutations (TAT to GGA) results in the amino acid substitution of glycine for tyrosine at position 682 (Y682G). Cre-mediated recombination removed the neo cassette. (J:166989)
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)
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 App Mutation:  105 strains or lines available
References
Original:  J:166989 Barbagallo AP, et al., Tyr(682) in the intracellular domain of APP regulates amyloidogenic APP processing in vivo. PLoS One. 2010;5(11):e15503
All:  4 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
11/12/2024
MGI 6.24
The Jackson Laboratory