Kcng3tm1e(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
Kcng3tm1e(KOMP)Wtsi |
Name: |
potassium voltage-gated channel, subfamily G, member 3; targeted mutation 1e, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:4451465 |
Gene: |
Kcng3 Location: Chr17:83893386-83939324 bp, - strand Genetic Position: Chr17, 53.64 cM
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Alliance: |
Kcng3tm1e(KOMP)Wtsi page
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IMPC: |
Kcng3 gene page |
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Mutant Cell Lines: |
EPD0527_3_B11, EPD0527_3_B12, EPD0527_3_C12, EPD0527_3_D10, EPD0527_3_D12, EPD0527_3_E09, EPD0527_3_F09, EPD0527_3_F10, EPD0527_3_H12 |
Germline Transmission: |
Earliest citation of germline transmission:
J:204812
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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) |
Mutation: |
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Insertion
Vector: L1L2_Bact_P
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Mutation details: The L1L2_Bact_P cassette was inserted at position 83896267 of Chromosome 17 upstream of the critical exon(s) (Build GRCm39). 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. 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: |
3 reference(s) |
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