1700029H14Riktm2b(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
1700029H14Riktm2b(KOMP)Wtsi |
Name: |
RIKEN cDNA 1700029H14 gene; targeted mutation 2b, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:5637012 |
Gene: |
1700029H14Rik Location: Chr8:13600733-13612461 bp, - strand Genetic Position: Chr8, 6.26 cM, cytoband A2
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Alliance: |
1700029H14Riktm2b(KOMP)Wtsi page
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IMPC: |
1700029H14Rik gene page |
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Mutant Cell Line: |
EPD0365_4_B04 |
Germline Transmission: |
Earliest citation of germline transmission:
J:204739
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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: Cre-mediated excision of the parental 1700029H14Riktm2a(KOMP)Wtsi allele resulted in the removal of the promoter-driven neomycin selection cassette and critical exon(s) leaving behind the inserted lacZ reporter sequence. 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:204739)
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Original: |
J:204739 International Knockout Mouse Consortium, MGI download of modified allele data from IKMC and creation of new knockout alleles. Database Download. 2014-2023; |
All: |
2 reference(s) |
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