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Apcstm1Smae
Targeted Allele Detail
Summary
Symbol: Apcstm1Smae
Name: amyloid P component, serum; targeted mutation 1, Shuichiro Maeda
MGI ID: MGI:2388056
Synonyms: sap-
Gene: Apcs  Location: Chr1:172721528-172722516 bp, - strand  Genetic Position: Chr1, 80.33 cM
Alliance: Apcstm1Smae page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:79398
Parent Cell Line:  CCE/EK.CCE (ES Cell)
Strain of Origin:  129S/SvEv-Gpi1c
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 1, 0.3 kb of flanking upstream sequences, and 50 bp of exon 2 were deleted and replaced with a PGK-neo cassette via homologous recombination. Absence of gene expression in homozygous mutant animals was confirmed by Western blot analysis of serum protein. (J:79398)
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Apcs Mutation:  21 strains or lines available
References
Original:  J:79398 Togashi S, et al., Serum amyloid P component enhances induction of murine amyloidosis. Lab Invest. 1997 Nov;77(5):525-31
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
04/16/2024
MGI 6.23
The Jackson Laboratory