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Cenpxtm1.1(KOMP)Wtsi
Targeted Allele Detail
Summary
Symbol: Cenpxtm1.1(KOMP)Wtsi
Name: centromere protein X; targeted mutation 1.1, Wellcome Trust Sanger Institute
MGI ID: MGI:5637204
Gene: Cenpx  Location: Chr11:120601768-120604564 bp, - strand  Genetic Position: Chr11, 84.45 cM, cytoband E2
Alliance: Cenpxtm1.1(KOMP)Wtsi page
IMPC: Cenpx gene page
Mutation
origin
Mutant Cell Line:  EPD0388_5_C02
Germline Transmission:  Earliest citation of germline transmission: J:204739
Parent Cell Line:  JM8A3.N1 (ES Cell)
Strain of Origin:  C57BL/6N-Atm1Brd
Project Collection: KOMP-CSD
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion     Vector: L1L2_Bact_P
 
Mutation detailsCre-mediated excision of the parental Stra13tm1(KOMP)Wtsi allele resulted in the removal of the neomycin selection cassette and critical exon(s) leaving behind the inserted lacZ reporter sequence. 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:204739)
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 Cenpx Mutation:  10 strains or lines available
References
Original:  J:204739 International Knockout Mouse Consortium, MGI download of modified allele data from IKMC and creation of new knockout alleles. Database Download. 2014-2023;
All:  1 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
01/20/2026
MGI 6.24
The Jackson Laboratory