- decreased lean body mass / IMPC
- decreased red blood cell distribution width / IMPC
- increased circulating alkaline phosphatase level / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal retina morphology / IMPC
- decreased neutrophil cell number / IMPC
- absent spleen / IMPC
- decreased grip strength / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
- embryonic lethality prior to organogenesis / IMPC
C57BL/6NCrl-Dicer1em3Psv/Ph
| Status | Available to order |
| EMMA ID | EM:07575 |
| Citation information | RRID:IMSR_EM:07575 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/6NCrl-Dicer1em3Psv/Ph |
| Alternative name | DcrMTdel |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Dicer1em3Psv |
| Gene/Transgene symbol | Dicer1 |
Information from provider
| Provider | Petr Svoboda |
| Provider affiliation | Dep. of Epigenetic Regulations, Institute of Molecular Genetics, v.v.i |
| Genetic information | TALEN-mediated deletion of MT-C (mouse transcript, type C) element in intron 6 of Dicer1 gene. |
| Phenotypic information | Sterility of homozygous females due to defects in oocyte maturation. Males and heterozygous females are fertile and without apparent phenotype. |
| Breeding history | Positive F0 mice were crossed with C57BL/6NCrl mice to get F1 generation. Transmitting F1 mice were intercrossed to obtain mice with all genotypes. |
| References |
|
| Homozygous fertile | no |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
| Animals used for archiving | heterozygous C57BL/6N males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome / Orphanet_404476
- Pleuropulmonary blastoma familial tumor susceptibility syndrome / Orphanet_284343
- Embryonal rhabdomyosarcoma / Orphanet_99757
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal angiogenesis / MGI
- small liver / MGI
- abnormal blood vessel morphology / MGI
- abnormal embryo development / MGI
- decreased embryo size / MGI
- absent vitelline blood vessels / MGI
- embryonic growth arrest / MGI
- female infertility / MGI
- no abnormal phenotype detected / MGI
- decreased susceptibility to viral infection / MGI
- increased susceptibility to viral infection / MGI
- no phenotypic analysis / MGI
- abnormal vitelline vascular remodeling / MGI
- increased B-1 B cell number / MGI
- decreased T cell number / MGI
- abnormal female meiosis / MGI
- reproductive system phenotype / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- decreased single-positive T cell number / MGI
- abnormal meiotic spindle morphology / MGI
- increased effector memory CD4-positive, alpha-beta T cell number / MGI
- increased central memory CD8 positive, alpha-beta T cell number / MGI
- increased effector memory CD8-positive, alpha-beta T cell number / MGI
- perinatal lethality, incomplete penetrance / MGI
- embryonic lethality between implantation and somite formation, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- decreased CD8-positive, naive alpha-beta T cell number / MGI
Literature references
- A retrotransposon-driven dicer isoform directs endogenous small interfering RNA production in mouse oocytes.;Flemr Matyas, Malik Radek, Franke Vedran, Nejepinska Jana, Sedlacek Radislav, Vlahovicek Kristian, Svoboda Petr, ;2013;Cell;155;807-16; 24209619
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