Setd5tm1c(EUCOMM)Wtsi
Targeted Allele Detail
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Symbol: |
Setd5tm1c(EUCOMM)Wtsi |
Name: |
SET domain containing 5; targeted mutation 1c, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:7438258 |
Synonyms: |
Setd5Fl |
Gene: |
Setd5 Location: Chr6:113054326-113130393 bp, + strand Genetic Position: Chr6, 52.73 cM, cytoband E3
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Alliance: |
Setd5tm1c(EUCOMM)Wtsi page
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IMPC: |
Setd5 gene page |
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Germline Transmission: |
Earliest citation of germline transmission:
J:314464
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Parent Cell Line: |
JM8.F6 (ES Cell)
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Strain of Origin: |
C57BL/6N
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Project Collection: |
EUCOMM
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Allele Type: |
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Targeted (Conditional ready) |
Mutation: |
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Insertion
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Mutation details: The L1L2_gt2 cassette was inserted at position 113086383 of Chromosome 6 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. An additional loxP site is inserted downstream of the targeted exon(s) at position 113088756. The critical exon(s) is/are thus flanked by loxP sites. The lacZ/neomycin sequence was removed via flp-mediated recombination generating a conditional ready (floxed) allele.
(J:314464)
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View phenotypes and curated references for all genotypes (concatenated display).
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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 Setd5 Mutation: |
122 strains or lines available
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Original: |
J:314464 Cheung MY, et al., Setd5 is required in cardiopharyngeal mesoderm for heart development and its haploinsufficiency is associated with outflow tract defects in mouse. Genesis. 2021 Aug;59(7-8):e23421 |
All: |
1 reference(s) |
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