Spata20tm1(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
Spata20tm1(KOMP)Wtsi |
Name: |
spermatogenesis associated 20; targeted mutation 1, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:4363195 |
Gene: |
Spata20 Location: Chr11:94369730-94376136 bp, - strand Genetic Position: Chr11, 58.9 cM
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IMPC: |
Spata20 gene page |
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Mutant Cell Lines: |
EPD0321_1_B05, EPD0321_1_B07, EPD0321_1_C07, EPD0321_1_E05, EPD0321_1_E06, EPD0321_1_E07, EPD0321_1_E08, EPD0321_1_G08, EPD0321_1_H06, EPD0321_1_H08 |
Germline Transmission: |
Unknown
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Parent Cell Line: |
JM8A1.N3 (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 3527 starting at position 94372417 and ending at position 94375944 of Chromosome 11 (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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