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Bin3tm1Gcp
Targeted Allele Detail
Summary
Symbol: Bin3tm1Gcp
Name: bridging integrator 3; targeted mutation 1, George C Prendergast
MGI ID: MGI:3512131
Gene: Bin3  Location: Chr14:70337538-70375413 bp, + strand  Genetic Position: Chr14, 36.21 cM, cytoband D1
Alliance: Bin3tm1Gcp page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:133313
Parent Cell Line:  AB2.1 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1b-m2
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsNeomycin resistance gene cassette replaces promoter and exon 1. Northern and Western blot analysis confirmed the absence of transcription and protein product. (J:133313)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 5 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 Bin3 Mutation:  18 strains or lines available
References
Original:  J:133313 Ramalingam A, et al., Bin3 deletion causes cataracts and increased susceptibility to lymphoma during aging. Cancer Res. 2008 Mar 15;68(6):1683-90
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
11/12/2024
MGI 6.24
The Jackson Laboratory