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Rad51ctm1Bcg
Targeted Allele Detail
Summary
Symbol: Rad51ctm1Bcg
Name: RAD51 paralog C; targeted mutation 1, Barbara C Godthelp
MGI ID: MGI:4461206
Synonyms: Rad51Csplice
Gene: Rad51c  Location: Chr11:87267471-87295780 bp, - strand  Genetic Position: Chr11, 52.08 cM
Alliance: Rad51ctm1Bcg page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:161642
Parent Cell Line:  IB10/E14IB10 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsIntron 5 was replaced with a neo cassette and a modified intron 5 in which a G to A nucleotide substitution 5 nucleotides into intron 5 altered the splice donor site of exon 5. (J:161642)
Phenotypes
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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 Rad51c Mutation:  24 strains or lines available
References
Original:  J:161642 Smeenk G, et al., Rad51C is essential for embryonic development and haploinsufficiency causes increased DNA damage sensitivity and genomic instability. Mutat Res. 2010 Jul 7;689(1-2):50-58
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
12/10/2024
MGI 6.24
The Jackson Laboratory