About   Help   FAQ
Nbntm2.1Zqw
Targeted Allele Detail
Nomenclature
Symbol: Nbntm2.1Zqw
Name: nibrin; targeted mutation 2.1, Zhao-Qi Wang
MGI ID: MGI:3578646
Synonyms: Nbndelta6
Gene: Nbn  Location: Chr4:15957925-15992589 bp, + strand  Genetic Position: Chr4, 6.66 cM, cytoband A
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:98316
Parent Cell Line:  E14.1 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
    Exon 6 was deleted via cre-mediated recombination. (J:98316)
Phenotypes
Loading...
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 Nbn Mutation:  38 strains or lines available
References
Original:  J:98316 Frappart PO, et al., An essential function for NBS1 in the prevention of ataxia and cerebellar defects. Nat Med. 2005 Jun;11(6):538-44
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
09/19/2017
MGI 6.10
The Jackson Laboratory