Flt3tm1.1Dgg
Targeted Allele Detail
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| Symbol: |
Flt3tm1.1Dgg |
| Name: |
FMS-like tyrosine kinase 3; targeted mutation 1.1, D Gilliland |
| MGI ID: |
MGI:7489690 |
| Synonyms: |
FltITDdelta |
| Gene: |
Flt3 Location: Chr5:147267551-147337299 bp, - strand Genetic Position: Chr5, 86.88 cM, cytoband G3
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| Alliance: |
Flt3tm1.1Dgg page
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| Allele Type: |
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Targeted (Humanized sequence) |
| Mutations: |
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Insertion, Intragenic deletion
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Mutation details: The human W51 mutation which causes the duplication of amino acid 595 to 601 (REYEYDL; AGAGAATATGAATATGATCTC) was inserted in-frame into exon 14, replacing the endogenous single copy (RDYEYDL; AGGGACTATGAATATGACCTT). A loxP site flanked neomycin selection cassette was inserted into intron 15, then was removed via Cre-mediated recombination in the germline.
(J:336420)
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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 Flt3 Mutation: |
94 strains or lines available
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| Original: |
J:336420 Li Y, et al., FLT3ITD drives context-specific changes in cell identity and variable interferon dependence during AML initiation. Blood. 2023 Mar 23;141(12):1442-1456 |
| All: |
1 reference(s) |
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