Spo11em1Jcs
Endonuclease-mediated Allele Detail
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Symbol: |
Spo11em1Jcs |
Name: |
SPO11 initiator of meiotic double stranded breaks; endonuclease-mediated mutation 1, John C Schimenti |
MGI ID: |
MGI:7623838 |
Synonyms: |
Spo11P306T |
Gene: |
Spo11 Location: Chr2:172819493-172835369 bp, + strand Genetic Position: Chr2, 95.64 cM, cytoband H4
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Alliance: |
Spo11em1Jcs page
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Strain of Origin: |
(FVB/NJ x B6(Cg)-Tyrc-2J/J)F1
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Allele Type: |
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Endonuclease-mediated (Humanized sequence) |
Mutation: |
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Single point mutation
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Mutation details: Proline codon 306 (CCA) in exon 11 was changed to threonine (ACA) (p.P306T) using an sgRNA (corresponding to GACCAAGCCATCTGATTGTT) and an ssODN template with CRISPR/Cas9 technology. The mutation is the equivalent of the same human mutation, represented by SNP rs185545661.
(J:279122)
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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
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Carrying any Spo11 Mutation: |
21 strains or lines available
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Original: |
J:279122 Tran TN, et al., A segregating human allele of SPO11 modeled in mice disrupts timing and amounts of meiotic recombination, causing oligospermia and a decreased ovarian reserve. Biol Reprod. 2019 Aug 1;101(2):347-359 |
All: |
1 reference(s) |
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