Trip11tm1Psmi
Targeted Allele Detail
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Symbol: |
Trip11tm1Psmi |
Name: |
thyroid hormone receptor interactor 11; targeted mutation 1, Patrick Smits |
MGI ID: |
MGI:6154130 |
Gene: |
Trip11 Location: Chr12:101800304-101879463 bp, - strand Genetic Position: Chr12, 51.3 cM, cytoband F1
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Alliance: |
Trip11tm1Psmi page
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Germline Transmission: |
Earliest citation of germline transmission:
J:253969
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
129/Sv
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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: A loxP site was inserted 671 bp upstream of exon 1 (which contains the ATG) and an FRT site-flanked neomycin selection cassette immediately followed by a loxP site was placed 1506 bp downstream of exon 1.
(J:253969)
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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 Trip11 Mutation: |
99 strains or lines available
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Original: |
J:253969 Bird IM, et al., The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects. Development. 2018 Jan 8;145(1):dev156588 |
All: |
1 reference(s) |
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