Del(XNxf2-Tmsb15a)2Jw
Targeted Allele Detail
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| Symbol: |
Del(XNxf2-Tmsb15a)2Jw |
| Name: |
deletion, Chr X, Jeremy Wang 2 |
| MGI ID: |
MGI:5584171 |
| Synonyms: |
DelB, Del(XNxf2-Tmsb15a)1Jw |
| Gene: |
Del(XNxf2-Tmsb15a)2Jw Location: unknown Genetic Position: ChrX, Syntenic
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| Allele Type: |
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Targeted (Null/knockout) |
| Mutations: |
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Insertion, Intergenic deletion, Intragenic deletion
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Del(XNxf2-Tmsb15a)2Jw involves 2 genes/genome features (Nxf2, Tmsb15a)
View all
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Mutation details: Nxf2tm1.1Jw /Y ES cells were electroporated with the pUP108 vector used to generate the Igs8tm1Jw allele which replaces a 5.6 kb intergenic region between Tmsb15a and Armcx5 with a floxed PGK-neo selection cassette, producing a targeted conditional allele with four loxP sites. Mice carrying this floxed allele were crossed with Actb-Cre mice to delete a 782 kb region on mouse chromosome X between Nxf2 and Tmsb15a.
(J:210663)
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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 Del(XNxf2-Tmsb15a)2Jw Mutation: |
0 strains or lines available
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| Original: |
J:210663 Zhou J, et al., Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome. Hum Mol Genet. 2014 Jul 15;23(14):3823-9 |
| All: |
1 reference(s) |
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Analysis Tools
