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Itgamtm1.1Dacb
Targeted Allele Detail
Summary
Symbol: Itgamtm1.1Dacb
Name: integrin alpha M; targeted mutation 1.1, Daniel C Bullard
MGI ID: MGI:6791321
Synonyms: 77His
Gene: Itgam  Location: Chr7:127661812-127717663 bp, + strand  Genetic Position: Chr7, 69.93 cM, cytoband F4
Alliance: Itgamtm1.1Dacb page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:281653
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Targeted (Humanized sequence)
Mutation:    Single point mutation
 
Mutation detailsA mutation was generated in exon 3 changing proline codon 77 (CCC) to histidine (CAC)(p.P77H). A loxP site was inserted into intron 2 and a second loxP site and an FRT site flanked neomycin resistance gene cassette into intron 3. The neo cassette was removed through subsequent flp-mediated recombination, leaving a conditional-ready allele with a floxed and mutated exon 3. The mutation mimics human SNP rs1143679 (p.R77H), which affects ligand binding of the encoded peptide. (J:281653)
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 Itgam Mutation:  49 strains or lines available
References
Original:  J:281653 Avery JT, et al., Mice expressing the variant rs1143679 allele of ITGAM (CD11b) show impaired DC-mediated T cell proliferation. Mamm Genome. 2019 Oct;30(9-10):245-259
All:  1 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
12/30/2025
MGI 6.24
The Jackson Laboratory