Efcab15tm1(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
Efcab15tm1(KOMP)Wtsi |
Name: |
EF-hand calcium binding domain 15; targeted mutation 1, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:4364587 |
Gene: |
Efcab15 Location: Chr11:103089770-103099374 bp, - strand Genetic Position: Chr11, 66.75 cM, cytoband D
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IMPC: |
Efcab15 gene page |
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Mutant Cell Line: |
EPD0272_7_D01 |
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 2502 starting at position 103090132 and ending at position 103092634 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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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 Efcab15 Mutation: |
11 strains or lines available
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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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