Summary | Mutation origin | Mutation description | Find Mice (IMSR) | References

Symbol:	Bcciptm1e(EUCOMM)Hmgu
Name:	BRCA2 and CDKN1A interacting protein; targeted mutation 1e, Helmholtz Zentrum Muenchen GmbH
MGI ID:	MGI:4436524
Gene:	Bccip  Location: Chr7:133311062-133322874 bp, + strand  Genetic Position: Chr7, 77.3 cM, cytoband F4
IMPC:	Bccip gene page

Mutant Cell Lines:	HEPD0517_2_A12, HEPD0517_2_B10
Germline Transmission:	Unknown
Parent Cell Line:	JM8.N4 (ES Cell)
Strain of Origin:	C57BL/6N
Project Collection:	EUCOMM

Allele Type:    Targeted (Null/knockout, Reporter) Mutation:    Insertion     Vector: L1L2_gt0   Mutation details: The L1L2_gt0 cassette was inserted at position 133318877 of Chromosome 7 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. Insertion of this cassette creates a reporter knockout mouse. Cre expression will remove the neomycin selection cassette. Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml (J:157065)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 0 strains available      Cell Lines: 1 line available
Carrying any Bccip Mutation:	24 strains or lines available

Original:	J:157065 Helmholtz Zentrum Muenchen GmbH, Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu). MGI Direct Data Submission. 2010-2015;
All:	1 reference(s)