- decreased body length / IMPC
- increased monocyte cell number / IMPC
- abnormal auditory brainstem response / IMPC
- decreased total retina thickness / IMPC
- abnormal eye anterior chamber depth / IMPC
- abnormal retina outer nuclear layer morphology / IMPC
- decreased lymphocyte cell number / IMPC
- hyperactivity / IMPC
- increased vertical activity / IMPC
- short tibia / IMPC
- increased circulating triglyceride level / IMPC
- decreased circulating creatinine level / IMPC
B6;129P2-Prmt2tm1Yah Cstbtm1Yah/+ +/Orl
Status | Available to order |
EMMA ID | EM:01810 |
Citation information | RRID:IMSR_EM:01810 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-Prmt2tm1Yah Cstbtm1Yah/+ +/Orl |
Alternative name | Cis (Hrmt1l1tm1Yah-Cstbtm1Yah) |
Strain type | Targeted Mutant Strains : Other targeted |
Allele/Transgene symbol | Prmt2tm1Yah, Cstbtm1Yah |
Gene/Transgene symbol | Prmt2, Cstb |
Information from provider
Provider | Yann HERAULT |
Provider affiliation | TAAM-CDTA UPS44, Institut de Transgenose, INTRAGENE |
Genetic information | Insertion by homologous recombination in ES cells using MICER of a targeting vector containing a loxP site at the Hrmt1l1 (Prmt2) locus and of a second vector, on the same homologous chromosome, containing a loxP site at the Cstb locus (cis configuration of the loxP sites on MMU10). |
Phenotypic information | No visible phenotype. |
Breeding history | Targeted mutation generated in 129P2 ES cells. Cells injected in C57BL/6 blastocysts. Backcrossed to C57BL/6, then intercrossed. |
References |
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Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Unverricht-Lundborg disease / Orphanet_308
- Autosomal recessive hypohidrotic ectodermal dysplasia / Orphanet_248
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- myoclonus / MGI
- abnormal cerebellum morphology / MGI
- cerebellum hypoplasia / MGI
- abnormal cornea morphology / MGI
- increased incidence of corneal inflammation / MGI
- corneal opacity / MGI
- corneal scarring / MGI
- ataxia / MGI
- impaired coordination / MGI
- abnormal gait / MGI
- abnormal apoptosis / MGI
- seizures / MGI
- nervous system phenotype / MGI
- abnormal nervous system physiology / MGI
- abnormal cerebellar granule cell morphology / MGI
- abnormal brain wave pattern / MGI
- abnormal eye physiology / MGI
- growth/size/body region phenotype / MGI
- behavior/neurological phenotype / MGI
- uveitis / MGI
- facial muscle spasm / MGI
- abnormal cell cycle / MGI
- abnormal vascular wound healing / MGI
- increased sacral vertebrae number / MGI
Literature references
- Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombination.;Duchon Arnaud, Besson Vanessa, Pereira Patricia Lopes, Magnol Laetitia, Hérault Yann, ;2008;Genetics;180;51-9; 18757940
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