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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
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View phenotypes 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:  14 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
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last database update
07/15/2014
MGI 5.18
The Jackson Laboratory