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Dbndd2tm1b(EUCOMM)Wtsi
Targeted Allele Detail
Nomenclature
Symbol: Dbndd2tm1b(EUCOMM)Wtsi
Name: dysbindin (dystrobrevin binding protein 1) domain containing 2; targeted mutation 1b, Wellcome Trust Sanger Institute
MGI ID: MGI:5513763
Gene: Dbndd2  Location: Chr2:164486106-164493319 bp, + strand  Genetic Position: Chr2, 85.17 cM
Mutation
origin
Mutant Cell Line:  EPD0821_1_A10
Germline Transmission:  Earliest citation of germline transmission: J:200814
Parent Cell Line:  JM8A3.N1 (ES Cell)
Strain of Origin:  C57BL/6N-Atm1Brd
Project Collection: EUCOMM
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion     Vector: L1L2_Bact_P
 
Mutation detailsCre excision of MGI:5051009 tm1a allele removes the promoter-driven neo and critical exon(s) leaving behind the lacZ reporter (J:200814)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 5 anatomical structures
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 Dbndd2 Mutation:  6 strains or lines available
References
Original:  J:200814 Toronto Centre for Phenogenomics, Strains and alleles submitted by Toronto Centre for Phenogenomics (NorCOMM2, funded by Genome Canada and Ontario Genomics Institute OGI-051). MGI Direct Data Submission. 2013;
All:  3 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
12/03/2019
MGI 6.14
The Jackson Laboratory