Cnot4tm1d(EUCOMM)Wtsi
Targeted Allele Detail
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| Symbol: |
Cnot4tm1d(EUCOMM)Wtsi |
| Name: |
CCR4-NOT transcription complex, subunit 4; targeted mutation 1d, Wellcome Trust Sanger Institute |
| MGI ID: |
MGI:6725736 |
| Gene: |
Cnot4 Location: Chr6:34999000-35110646 bp, - strand Genetic Position: Chr6, 15.2 cM, cytoband B1
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| Alliance: |
Cnot4tm1d(EUCOMM)Wtsi page
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| IMPC: |
Cnot4 gene page |
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| Mutant Cell Line: |
EPD0682_3_G11 |
| Germline Transmission: |
Earliest citation of germline transmission:
J:307645
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| Parent Cell Line: |
JM8A3.N1 (ES Cell)
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| Strain of Origin: |
C57BL/6N-Atm1Brd
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| Project Collection: |
EUCOMM
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| Allele Type: |
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Targeted (Null/knockout) |
| Mutations: |
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Insertion, Intragenic deletion
Vector: L1L2_Bact_P
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Mutation details: The L1L2_Bact_P cassette was inserted at position 35056769 of Chromosome 6 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of the targeted exon(s) at position 35057701. The critical exon(s) is/are thus flanked by loxP sites. A "conditional ready" (floxed) allele was created by flp recombinase expression in mice carrying this allele. Subsequent cre expression resulted in a knockout mouse. 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:307645)
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View phenotypes and curated references for all genotypes (concatenated display).
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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 Cnot4 Mutation: |
50 strains or lines available
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| Original: |
J:307645 Dai XX, et al., The CNOT4 Subunit of the CCR4-NOT Complex is Involved in mRNA Degradation, Efficient DNA Damage Repair, and XY Chromosome Crossover during Male Germ Cell Meiosis. Adv Sci (Weinh). 2021 May;8(10):2003636 |
| All: |
1 reference(s) |
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