- abnormal heart morphology / IMPC
- enlarged heart / IMPC
- abnormal spleen morphology / IMPC
- enlarged lymph nodes / IMPC
- abnormal thymus morphology / IMPC
- enlarged thymus / IMPC
- abnormal skeletal muscle morphology / IMPC
- abnormal uterus morphology / IMPC
- abnormal skin morphology / IMPC
- abnormal digit morphology / IMPC
- abnormal lymph node morphology / IMPC
- thick ventricular wall / IMPC
- decreased heart rate / IMPC
- increased hemoglobin content / IMPC
- increased heart left ventricle size / IMPC
- preweaning lethality, complete penetrance / IMPC
- embryonic lethality prior to organogenesis / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
C57BL/6NCrl-Atp1a1em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:12889 |
Citation information | RRID:IMSR_EM:12889 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 | C57BL/6NCrl-Atp1a1em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Atp1a1em1(IMPC)Ccpcz |
Gene/Transgene symbol | Atp1a1 |
Information from provider
Provider | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal dominant Charcot-Marie-Tooth disease type 2DD / Orphanet_521414
- Primary hypomagnesemia-refractory seizures-intellectual disability syndrome / Orphanet_564178
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal spleen morphology / IMPC
- abnormal lymph node morphology / IMPC
- abnormal skin morphology / IMPC
- thick ventricular wall / IMPC
- increased hemoglobin content / IMPC
- abnormal digit morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal uterus morphology / IMPC
- enlarged heart / IMPC
- increased heart left ventricle size / IMPC
- embryonic lethality prior to organogenesis / IMPC
- abnormal heart morphology / IMPC
- enlarged thymus / IMPC
- abnormal skeletal muscle morphology / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
- decreased heart rate / IMPC
- enlarged lymph nodes / IMPC
- abnormal thymus morphology / IMPC
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).