- enlarged heart / MGI
- open neural tube / MGI
- wavy neural tube / MGI
- abnormal placenta morphology / MGI
- placental labyrinth hypoplasia / MGI
- abnormal visceral yolk sac morphology / MGI
- embryonic growth arrest / MGI
- pericardial edema / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal proerythroblast morphology / MGI
- decreased erythrocyte cell number / MGI
- no phenotypic analysis / MGI
- abnormal forebrain development / MGI
- pallor / MGI
- embryonic growth retardation / MGI
- small placenta / MGI
- cellular phenotype / MGI
- neonatal lethality, complete penetrance / MGI
- prenatal lethality, complete penetrance / MGI
- embryonic lethality between implantation and somite formation, complete penetrance / MGI
C57BL/6-Ago2em1Jghy/H
| Status | Available to order |
| EMMA ID | EM:13149 |
| Citation information | RRID:IMSR_EM:13149 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 | C57BL/6-Ago2em1Jghy/H |
| Alternative name | Ago2 S388A |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Ago2em1Jghy |
| Gene/Transgene symbol | Ago2 |
Information from provider
| Provider | Jonathan Hanley |
| Provider affiliation | Biochemistry, University of Bristol |
| Genetic information | Point mutation in the argonaute 2 (Ago2) gene made by CRISPR/Cas9 gene editing: AGT (Ser) to GCT (Ala), Ser 388 mutated to Ala. |
| Phenotypic information | Homozygous:UnknownHeterozygous:Grossly normal, but detailed characterisation not yet carried out, since phenotyping still ongoing. Please enquire for more information. |
| Breeding history | F0 animal was bred onto C57BL/6J and the resulting offspring were then bred again to C57BL/6J to generate the F2 animals. |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Non-specific syndromic intellectual disability / Orphanet_528084
MGI phenotypes (gene matching)
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