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Mcm10tm1(NCOM)Cmhd
Targeted Allele Detail
Summary
Symbol: Mcm10tm1(NCOM)Cmhd
Name: minichromosome maintenance 10 replication initiation factor; targeted mutation 1, Centre for Modelling Human Disease
MGI ID: MGI:4839016
Gene: Mcm10  Location: Chr2:4995535-5017602 bp, - strand  Genetic Position: Chr2, 3.12 cM, cytoband A1
Alliance: Mcm10tm1(NCOM)Cmhd page
IMPC: Mcm10 gene page
Mutation
origin
Mutant Cell Lines:  N00006P0_C_6T_A5, N00006P0_C_6T_B5, N00006P0_C_6T_C5, N00006P0_C_6T_D5, N00006P0_C_6T_E5, N00006P0_C_6T_F5, N00006P0_C_6T_G5, N00006P0_C_6T_H5
Germline Transmission:  Earliest citation of germline transmission: J:165965
Parent Cell Line:  C2 (Tcp) (ES Cell)
Strain of Origin:  C57BL/6N
Project Collection: NorCOMM
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion     Vector: L1L2_NTARU-1
 
Mutation detailsThe insertion of NorCOMM cassette pNTARU created a deletion of size 436bp between positions 5011054-5011490 of Chromosome 2 (Build GRCm39). This deletion results in the removal of functionally critical exon(s). The cassette is composed of an F3 site followed by a universal inverse PCR primer site and a splice acceptor lacZ-neomycin phosphotransferase fusion (beta-geo) sequence. This is followed by a PhiC31 attP site and a puromycin sequence that is not active unless a promoter is inserted by PhiC31 at the attP site. The cassette is finished with an FRT site. Variations of this allele can be made using PhiC31 docking and subsequent cloning (Nagy et al., 2009. Methods Mol. Biol. 530:365-78). (J:165963)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Mcm10 Mutation:  55 strains or lines available
References
Original:  J:165963 Centre for Modeling Human Disease, Alleles produced for the NorCOMM project by the Centre for Modeling Human Disease (Cmhd), Institute of Biomaterials & Biomedical Engineering, University of Toronto. MGI Direct Data Submission. 2010;
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
12/10/2024
MGI 6.24
The Jackson Laboratory