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Itgamm2Btlr
Chemically induced Allele Detail
Summary
Symbol: Itgamm2Btlr
Name: integrin alpha M; mutation 2, Bruce Beutler
MGI ID: MGI:6285545
Synonyms: obscured
Gene: Itgam  Location: Chr7:127661812-127717663 bp, + strand  Genetic Position: Chr7, 69.93 cM, cytoband F4
Alliance: Itgamm2Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU-induced C to T transition at base pair 128,081,634 (v38) on chromosome 7, or base pair 18,995 in the GenBank genomic region NC_000073. The mutation corresponds to residue 837 in the mRNA sequence NM_001082960 within exon 8 of 30 total exons. The mutation results in an alanine to valine substitution at position 245 (A245V) in the CD11b protein. (J:272532)
Inheritance:    Recessive
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 Itgam Mutation:  47 strains or lines available
Notes
https://mutagenetix.utsouthwestern.edu/phenotypic/phenotypic_rec.cfm?pk=3757
References
Original:  J:272532 Zhong X, et al., Mutagenetix entry for obscured. MGI Direct Data Submission. 2019;
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
04/23/2024
MGI 6.23
The Jackson Laboratory