Ptpn2tm2.1Ttig
Targeted Allele Detail
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| Symbol: |
Ptpn2tm2.1Ttig |
| Name: |
protein tyrosine phosphatase, non-receptor type 2; targeted mutation 2.1, Tony Tiganis |
| MGI ID: |
MGI:5436249 |
| Synonyms: |
Ptpn2ex2- |
| Gene: |
Ptpn2 Location: Chr18:67798581-67857665 bp, - strand Genetic Position: Chr18, 40.06 cM
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| Alliance: |
Ptpn2tm2.1Ttig page
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Runtiness of Ptpn2tm1Mtr/Ptpn2tm1Mtr and Ptpn2tm2.1Ttig/Ptpn2tm2.1Ttig mice
Show the 2 phenotype image(s) involving this allele.
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| Germline Transmission: |
Earliest citation of germline transmission:
J:186843
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| Parent Cell Line: |
Bruce 4 (ES Cell)
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| Strain of Origin: |
B6.Cg-Thy1a
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| Allele Type: |
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Targeted (Null/knockout) |
| Mutations: |
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Insertion, Intragenic deletion
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Mutation details: A loxP site was inserted upstream of exon 2 and an FRT flanked pgk-neo cassette and loxP site were inserted downstream of exon 2 via homologous recombination. Cre mediated recombination removed exon 2 and the pgk-neo cassette. Western blot analysis confirmed the absence of full length protein in tissues from homozygous mice.
(J:186843)
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Generation of the Ptpn2tm2.1Ttig allele |
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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 Ptpn2 Mutation: |
42 strains or lines available
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| Original: |
J:186843 Wiede F, et al., Strain-dependent differences in bone development, myeloid hyperplasia, morbidity and mortality in ptpn2-deficient mice. PLoS One. 2012;7(5):e36703 |
| All: |
4 reference(s) |
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