Bmftm1(KOMP)Wtsi
Targeted Allele Detail
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| Symbol: |
Bmftm1(KOMP)Wtsi |
| Name: |
BCL2 modifying factor; targeted mutation 1, Wellcome Trust Sanger Institute |
| MGI ID: |
MGI:4419589 |
| Gene: |
Bmf Location: Chr2:118359238-118380168 bp, - strand Genetic Position: Chr2, 59.4 cM, cytoband E5
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| IMPC: |
Bmf gene page |
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| Mutant Cell Lines: |
EPD0391_5_A03, EPD0391_5_B02, EPD0391_5_B04, EPD0391_5_C02, EPD0391_5_C04, EPD0391_5_D01, EPD0391_5_F04, EPD0391_5_G03, EPD0391_5_G04, EPD0391_5_H03 |
| Germline Transmission: |
Unknown
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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: |
KOMP-CSD
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| Allele Type: |
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Targeted (Null/knockout, Reporter) |
| Mutations: |
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Insertion, Intragenic deletion
Vector: L1L2_Bact_P
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Mutation details: The insertion of the L1L2_Bact_P cassette created a deletion of size 4190 starting at position 118375495 and ending at position 118379685 of Chromosome 2 (Genome Build GRCm39). This deletion results in the removal of functionally critical exon(s). 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.
(J:148605, J:173534)
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| Original: |
J:148605 Wellcome Trust Sanger Institute, Alleles produced for the KOMP project by the Wellcome Trust Sanger Institute. MGI Direct Data Submission. 2009; |
| All: |
2 reference(s) |
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