- abnormal embryo development / MGI
- abnormal ectoderm development / MGI
- abnormal mesoderm development / MGI
- decreased embryo size / MGI
- embryonic growth arrest / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal extraembryonic tissue morphology / MGI
- abnormal gastrulation movements / MGI
- disorganized extraembryonic tissue / MGI
- abnormal trophoblast layer morphology / MGI
- abnormal extraembryonic mesoderm development / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality between somite formation and embryo turning, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal proamniotic cavity morphology / MGI
- abnormal amniotic cavity morphology / MGI
- absent ectoplacental cavity / MGI
- small proamniotic cavity / MGI
- absent extraembryonic coelom / MGI
- small amniotic cavity / MGI
- embryonic-extraembryonic boundary constriction / MGI
B6.129P2-Tln1tm4.1Crit/CritH
Status | Available to order |
EMMA ID | EM:04999 |
Citation information | RRID:IMSR_EM:04999 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | B6.129P2-Tln1tm4.1Crit/CritH |
Alternative name | Tln1(tm4.1Crit) |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Tln1tm4.1Crit |
Gene/Transgene symbol | Tln1 |
Information from provider
Provider | Sue Monkley |
Provider affiliation | Biomedical Services, University of Leicester |
Additional owner | Prof David Critchley, Dept of Biochemistry, University of Leicester, Leicester, UK |
Genetic information | Conditional talin 1 allele with loxP sites upstream of the 1st coding exon and downstream of the 4th coding exon. Cre-mediated deletion of exons 1-4 results in a null allele. |
Phenotypic information | The homozygous floxed Tln1 mice are viable and fertile and do not exhibit evidence of any phenotype. |
Breeding history | The line was generated with a floxed neo cassette that was deleted by crossing to cre-deleter mice. The allele was then backcrossed to C57BL/6 and then intercrossed to generate homozygous mice. The allele is maintained as homozygous. |
References |
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Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Animals used for archiving | homozygous C57BL/6.129/Sv males |
Breeding at archiving centre | Males were archived upon arrival. No breeding was performed at the archiving centre. |
Disease and phenotype information
MGI phenotypes (gene matching)
Literature references
- Talin is required for integrin-mediated platelet function in hemostasis and thrombosis.;Petrich Brian G, Marchese Patrizia, Ruggeri Zaverio M, Spiess Saskia, Weichert Rachel A M, Ye Feng, Tiedt Ralph, Skoda Radek C, Monkley Susan J, Critchley David R, Ginsberg Mark H, ;2007;The Journal of experimental medicine;204;3103-11; 18086863
- Loss of talin1 in platelets abrogates integrin activation, platelet aggregation, and thrombus formation in vitro and in vivo.;Nieswandt Bernhard, Moser Markus, Pleines Irina, Varga-Szabo David, Monkley Sue, Critchley David, Fässler Reinhard, ;2007;The Journal of experimental medicine;204;3113-8; 18086864
- Talin 1 and 2 are required for myoblast fusion, sarcomere assembly and the maintenance of myotendinous junctions.;Conti Francesco J, Monkley Sue J, Wood Malcolm R, Critchley David R, Müller Ulrich, ;2009;Development (Cambridge, England);136;3597-606; 19793892
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