- 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
129S2.Cg-Ago2tm1.1Doca/Cnrm
Status | Available to order |
EMMA ID | EM:07112 |
Citation information | RRID:IMSR_EM:07112 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 | 129S2.Cg-Ago2tm1.1Doca/Cnrm |
Alternative name | 129S2/SvHsd - Ago2S388A |
Strain type | Targeted Mutant Strains : Point mutation |
Allele/Transgene symbol | Ago2tm1.1Doca |
Gene/Transgene symbol | Ago2 |
Information from provider
Provider | Donal O'Carroll |
Provider affiliation | Mouse Biology Unit, European Molecular Biology Laboratory |
Genetic information | Two point mutations in exon 10, converting Serine 388 in an Alanine residue. Residual LoxP site between exon 8 and 9 due to removal of neomycin resistance cassette. |
Phenotypic information | Homozygous mice for the point mutation are born with subMendelian frequencies in this genetic background. |
Breeding history | The mice were backcrossed 9 times with 129S2/SvHsd mice from Harlan. |
References | None available |
Homozygous fertile | yes |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
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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