- abnormal lens morphology / IMPC
- abnormal retina morphology / IMPC
- increased startle reflex / IMPC
- abnormal motor coordination/balance / IMPC
- abnormal retina vasculature morphology / IMPC
- decreased mean platelet volume / IMPC
- abnormal retina blood vessel morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Jmjd6tm1b(EUCOMM)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:08088 |
International strain name | C57BL/6N-Jmjd6tm1b(EUCOMM)Wtsi/Ieg |
Alternative name | EPD0158_3_A11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Jmjd6tm1b(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. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele (Gt(ROSA)26Sor |
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 |
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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