- abnormal motor coordination/balance / IMPC
- decreased mean platelet volume / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal retina vasculature morphology / IMPC
- increased total body fat amount / IMPC
- abnormal lens morphology / IMPC
- abnormal retina morphology / IMPC
- increased startle reflex / IMPC
- abnormal retina blood vessel morphology / IMPC
- increased NK cell number / IMPC
B6.Cg-Jmjd6tm1.1Gbf/Ieg
Status | Available to order |
EMMA ID | EM:04329 |
Citation information | RRID:IMSR_EM:04329 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.Cg-Jmjd6tm1.1Gbf/Ieg |
Alternative name | C57Bl/6J-Jmjd6 tm1.1 Gbf |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Jmjd6tm1.1Gbf |
Gene/Transgene symbol | Jmjd6 |
Information from provider
Provider | Andreas Lengeling |
Provider affiliation | Tierhaus TEE, Helmholtz Centre for Infection Research |
Genetic information | Intragenic deletion of exon 1 and 2. This allele was created by removing the floxed neomycin cassette from Jmjd6tm1Gbf mice by crossing them to a CMV cre deleter line. |
Phenotypic information | Mice homozygous for disruption in this gene show neonatal lethality. Abnormalities are observed in the nervous, cardiovascular, digestive, renal, hematopoietic, and immune systems. |
Breeding history | The mutation was generated in Bruce 4 ES cells. Germline chimeras were bred to C57BL/6J mice to establish a breeding colony. Since then the strain has been maintained by brother x sister matings (>15 generations). |
References |
|
Homozygous fertile | no |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6J males, wild-type C57BL/6J females |
Stage of embryos | 2-cell |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- ventricular septal defect / MGI
MGI phenotypes (gene matching)
- decreased hematocrit / MGI
- abnormal erythropoiesis / MGI
- double outlet right ventricle / MGI
- abnormal intestine morphology / MGI
- abnormal pulmonary artery morphology / MGI
- abnormal kidney development / MGI
- liver hypoplasia / MGI
- abnormal thymus development / MGI
- small thymus / MGI
- abnormal brain development / MGI
- exencephaly / MGI
- abnormal lung development / MGI
- anophthalmia / MGI
- cyanosis / MGI
- abnormal apoptosis / MGI
- skin edema / MGI
- impaired macrophage phagocytosis / MGI
- thymus hypoplasia / MGI
- respiratory failure / MGI
- abnormal respiratory system morphology / MGI
- decreased hemoglobin content / MGI
- no phenotypic analysis / MGI
- pallor / MGI
- impaired macrophage chemotaxis / MGI
- thin myocardium compact layer / MGI
- decreased fetal size / MGI
- fetal growth retardation / MGI
- abnormal heart ventricle morphology / MGI
- cellular phenotype / MGI
- increased nucleated erythrocyte cell number / MGI
- abnormal blood homeostasis / MGI
- cleft secondary palate / MGI
- ventricular septal defect / MGI
- myocardial trabeculae hypoplasia / MGI
- abnormal macrophage activation involved in immune response / MGI
- neonatal lethality, complete penetrance / MGI
- perinatal lethality, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- abnormal head shape / MGI
Literature references
- The phosphatidylserine receptor has essential functions during embryogenesis but not in apoptotic cell removal.;Böse Jens, Gruber Achim D, Helming Laura, Schiebe Stefanie, Wegener Ivonne, Hafner Martin, Beales Marianne, Köntgen Frank, Lengeling Andreas, ;2004;Journal of biology;3;15; 15345036
- Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique.;Schneider Jürgen E, Böse Jens, Bamforth Simon D, Gruber Achim D, Broadbent Carol, Clarke Kieran, Neubauer Stefan, Lengeling Andreas, Bhattacharya Shoumo, ;2004;BMC developmental biology;4;16; 15615595
- Genomic structure and expression of Jmjd6 and evolutionary analysis in the context of related JmjC domain containing proteins.;Hahn Phillip, Böse Jens, Edler Stefanie, Lengeling Andreas, ;2008;BMC genomics;9;293; 18564434