Fam222btm1e(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
Fam222btm1e(KOMP)Wtsi |
Name: |
family with sequence similarity 222, member B; targeted mutation 1e, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:4362516 |
Gene: |
Fam222b Location: Chr11:77985486-78047526 bp, + strand Genetic Position: Chr11, 46.74 cM
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IMPC: |
Fam222b gene page |
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Mutant Cell Lines: |
EPD0017_3_A10, EPD0017_3_A11, EPD0017_3_A12, EPD0017_3_E11, EPD0017_3_G12, EPD0019_1_B10, EPD0019_1_B12, EPD0019_1_C10, EPD0019_1_C11, EPD0019_1_D11, EPD0019_1_D12, EPD0019_1_G11, EPD0019_1_H10, EPD0019_1_H11 |
Germline Transmission: |
Unknown
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Parent Cell Line: |
JM8 (ES Cell)
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Strain of Origin: |
C57BL/6N
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Project Collection: |
KOMP-CSD
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Allele Type: |
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Targeted (Null/knockout, Reporter) |
Mutation: |
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Insertion
Vector: L1L2_st0
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Mutation details: The L1L2_st0 cassette was inserted at position 78033480 of Chromosome 11 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. Insertion of this cassette creates a reporter knockout mouse. Cre expression will remove the neomycin selection cassette. 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: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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