- decreased circulating total protein level / IMPC
- increased circulating bilirubin level / IMPC
- decreased circulating HDL cholesterol level / IMPC
- decreased exploration in new environment / IMPC
- decreased circulating unsaturated transferrin level / IMPC
- decreased circulating cholesterol level / IMPC
- increased startle reflex / IMPC
- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Pkn2tm1a(KOMP)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:09415 |
International strain name | C57BL/6N-Pkn2tm1a(KOMP)Wtsi/Ieg |
Alternative name | EPD0319_7_G05 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Pkn2tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Pkn2 |
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 KOMP ES clone EPD0319_7_G05. 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/6NTac |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- abnormal vascular development / MGI
- open neural tube / MGI
- abnormal somite development / MGI
- abnormal embryo turning / MGI
- absent vitelline blood vessels / MGI
- disorganized yolk sac vascular plexus / MGI
- pericardial edema / MGI
- abnormal developmental patterning / MGI
- abnormal neural tube morphology / MGI
- abnormal neural crest cell migration / MGI
- abnormal vitelline vasculature morphology / MGI
- absent pharyngeal arches / MGI
- abnormal rostral-caudal body axis extension / MGI
- abnormal neural fold formation / MGI
- abnormal mesenchyme morphology / MGI
- craniorachischisis / MGI
- delayed heart looping / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal fibroblast proliferation / MGI
- abnormal head development / MGI
- abnormal vascular plexus formation / MGI
- abnormal germ layer morphology / MGI
MGI phenotypes (gene matching)
- abnormal vascular development / MGI
- open neural tube / MGI
- abnormal somite development / MGI
- abnormal embryo turning / MGI
- absent vitelline blood vessels / MGI
- disorganized yolk sac vascular plexus / MGI
- pericardial edema / MGI
- abnormal developmental patterning / MGI
- abnormal neural tube morphology / MGI
- abnormal neural crest cell migration / MGI
- abnormal vitelline vasculature morphology / MGI
- absent pharyngeal arches / MGI
- abnormal rostral-caudal body axis extension / MGI
- abnormal neural fold formation / MGI
- abnormal mesenchyme morphology / MGI
- craniorachischisis / MGI
- delayed heart looping / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal fibroblast proliferation / MGI
- abnormal head development / MGI
- abnormal vascular plexus formation / MGI
- abnormal germ layer morphology / MGI
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