Ercc6ltm1(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
Ercc6ltm1(KOMP)Wtsi |
Name: |
excision repair cross-complementing rodent repair deficiency complementation group 6 like; targeted mutation 1, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:5424641 |
Gene: |
Ercc6l Location: ChrX:101186426-101200697 bp, - strand Genetic Position: ChrX, 45.16 cM
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IMPC: |
Ercc6l gene page |
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Mutant Cell Lines: |
EPD0673_3_B04, EPD0673_3_C01, EPD0673_3_C02, EPD0673_3_C03, EPD0673_3_E01, EPD0673_3_F01, EPD0673_3_G03, EPD0673_3_H02 |
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 3738 starting at position 101186724 and ending at position 101190462 of Chromosome X (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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