Fam13ctm1(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
Fam13ctm1(KOMP)Wtsi |
Name: |
family with sequence similarity 13, member C; targeted mutation 1, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:4431450 |
Gene: |
Fam13c Location: Chr10:70276311-70394566 bp, + strand Genetic Position: Chr10, 36.68 cM, cytoband B5.2
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IMPC: |
Fam13c gene page |
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Mutant Cell Lines: |
EPD0447_1_E07, EPD0447_1_F07, EPD0447_1_F08, EPD0447_1_F09 |
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 701 starting at position 70286490 and ending at position 70287191 of Chromosome 10 (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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