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Spo11tm2.1Rdco
Targeted Allele Detail
Summary
Symbol: Spo11tm2.1Rdco
Name: SPO11 initiator of meiotic double stranded breaks; targeted mutation 2.1, R Daniel Camerini-Otero
MGI ID: MGI:5490537
Synonyms: Spo11FF, Spo11YY137,138FF
Gene: Spo11  Location: Chr2:172819493-172835369 bp, + strand  Genetic Position: Chr2, 95.64 cM, cytoband H4
Alliance: Spo11tm2.1Rdco page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:194067
Parent Cell Line:  TC1/TC-1 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 5 was replaced with a modified exon 5 in which nucleotide substitutions result in the amino acid substitutions of phenylalanine for tyrosine at positions 137 and 138 (Y137F, Y138F). Cre-mediated recombination removed the floxed neomycin resistance cassette that was inserted downstream of exon 8. (J:194067)
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 Spo11 Mutation:  20 strains or lines available
References
Original:  J:194067 Boateng KA, et al., Homologous pairing preceding SPO11-mediated double-strand breaks in mice. Dev Cell. 2013 Jan 28;24(2):196-205
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
04/23/2024
MGI 6.23
The Jackson Laboratory