C57BL/6NTac-Jmjd6tm1a(EUCOMM)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:04584 |
International strain name | C57BL/6NTac-Jmjd6tm1a(EUCOMM)Wtsi/Ieg |
Alternative name | EPD0158_3_A11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Jmjd6tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Jmjd6 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0158_3_A11. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTacUSA, wild-type C57BL/6NTacUSA |
Stage of embryos | 2-cell |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- 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
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
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