Adamtsl2tm1b(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
Adamtsl2tm1b(KOMP)Wtsi |
Name: |
ADAMTS-like 2; targeted mutation 1b, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:5696789 |
Gene: |
Adamtsl2 Location: Chr2:26969391-26998993 bp, + strand Genetic Position: Chr2, Syntenic
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Alliance: |
Adamtsl2tm1b(KOMP)Wtsi page
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IMPC: |
Adamtsl2 gene page |
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Germline Transmission: |
Earliest citation of germline transmission:
J:221347
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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: |
KOMP-CSD
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Allele Type: |
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Targeted (Null/knockout, Reporter) |
Mutations: |
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Insertion, Intragenic deletion
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Mutation details: The loxP-flanked neomycin selection cassette and exon 5 of Adamtsl2tm1a(KOMP)Wtsi were deleted via cre-mediated recombination. This allele expresses the lacZ gene under the control of the endogenous gene promoter.
(J:221347)
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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 Adamtsl2 Mutation: |
33 strains or lines available
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Original: |
J:221347 Hubmacher D, et al., Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia - a novel mouse model providing insights into geleophysic dysplasia. Dis Model Mech. 2015 May 1;8(5):487-99 |
All: |
3 reference(s) |
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