- 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;CBA-Tln1em1Flmg/Flmg
| Status | Available to order |
| EMMA ID | EM:13074 |
| Citation information | RRID:IMSR_EM:13074 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;CBA-Tln1em1Flmg/Flmg |
| Alternative name | Talin1 C-mutant |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Tln1em1Flmg |
| Gene/Transgene symbol | Tln1 |
Information from provider
| Provider | Transgenics Facility B.S.R.C. |
| Provider affiliation | B.S.R.C. "Alexander Fleming" |
| Genetic information | Mice with a deletion of exons 55-57 of talin 1 gene were generated using CRISPR/Cas9 technology. Two guide RNAs were designed to target sequences outside of the selected area. A ssODN template consisting of two 60 bp fragments at each of the outer sides of the Cas9 cutting edges was used producing a deletion of 1033 bp. The CRISPR components were introduced into zygotes via the embryo electroporation method. |
| Phenotypic information | Homozygous:Embryonic lethalHeterozygous:No observable phenotype |
| Breeding history | The colony has been maintained by backcrossing talin 1 C mutant heterozygous mice to C57BL/6J mice for six generations; talin 1 C mutant homozygotes are embryonic lethal. |
| References | None available |
| Homozygous fertile | no |
| Homozygous viable | no |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | B.S.R.C. Alexander Fleming, Vari, Greece |
| Animals used for archiving | heterozygous CBA x C57BL/6 males, wild-type C57BL/6J females |
| Stage of embryos | Morula |
Disease and phenotype information
MGI phenotypes (gene matching)
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