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Ighmtm1Bhe
Targeted Allele Detail
Summary
Symbol: Ighmtm1Bhe
Name: immunoglobulin heavy constant mu; targeted mutation 1, Birgitta Heyman
MGI ID: MGI:5297544
Synonyms: Cmu13
Gene: Ighm  Location: Chr12:113382446-113386350 bp, - strand  Genetic Position: Chr12, 62.1 cM, cytoband F1-2
Alliance: Ighmtm1Bhe page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:177421
Parent Cell Line:  Bruce 4 (ES Cell)
Strain of Origin:  B6.Cg-Thy1a
Mutation
description
Allele Type:    Targeted (Not Specified)
Mutations:    Insertion, Single point mutation
 
Mutation detailsA C to T point mutation was introduced into the gene coding for the third C domain of the mu-heavy chain causing the amino acid encoded by codon 436 to change from proline to serine. A floxed neomycin was inserted as well. This neo cassette was subsequently excised from correctly targeted mice. (J:177421, J:178135, J:178136)
Generation of the Ighmtm1Bhe allele
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 Ighm Mutation:  56 strains or lines available
References
Original:  J:177421 Rutemark C, et al., Requirement for complement in antibody responses is not explained by the classic pathway activator IgM. Proc Natl Acad Sci U S A. 2011 Oct 25;108(43):E934-42
All:  5 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
10/29/2024
MGI 6.24
The Jackson Laboratory