- 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
- 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-Tln1tm1Crit/CritH
| Status | Available to order |
| EMMA ID | EM:00185 |
| Citation information | RRID:IMSR_EM:00185 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-Tln1tm1Crit/CritH |
| Alternative name | Tln1((hyg/+)/C57) |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Tln1tm1Crit |
| Gene/Transgene symbol | Tln1 |
Information from provider
| Provider | Martin FRAY |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | The endogenous locus was disrupted by insertion of a hygromycin selection cassette. Codons 37 through 66 were deleted by the insertion. |
| Phenotypic information | Talin binds directly to selected integrin beta-subunit cytodomains and to F-actin. This interaction is disrupted in mice homozygous for this knock-out allele. |
| Breeding history | The original founder stock has been repeatedly (more than 8 generations) backcrossed to C57BL/6J. |
| References |
|
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- 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
Literature references
- Disruption of the talin gene arrests mouse development at the gastrulation stage.;Monkley S J, Zhou X H, Kinston S J, Giblett S M, Hemmings L, Priddle H, Brown J E, Pritchard C A, Critchley D R, Fässler R, ;2000;Developmental dynamics : an official publication of the American Association of Anatomists;219;560-74; 11084655
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