- abnormal heart morphology / IMPC
- enlarged heart / IMPC
- abnormal stomach morphology / IMPC
- abnormal spleen morphology / IMPC
- small spleen / IMPC
- enlarged lymph nodes / IMPC
- abnormal thymus morphology / IMPC
- enlarged thymus / IMPC
- abnormal testis morphology / IMPC
- small testis / IMPC
- small seminal vesicle / IMPC
- decreased body weight / IMPC
- abnormal seminal vesicle morphology / IMPC
- abnormal skin morphology / IMPC
- abnormal tooth morphology / IMPC
- abnormal lymph node morphology / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- vertebral transformation / IMPC
- enlarged stomach / IMPC
- abnormal vertebral arch morphology / IMPC
- increased eosinophil cell number / IMPC
- decreased lymphocyte cell number / IMPC
- abnormal zygomatic bone morphology / IMPC
- increased lung tissue damping / IMPC
- abnormal tooth color / IMPC
- absent teeth / IMPC
C57BL/6NCrl-Amelxem1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:12626 |
Citation information | RRID:IMSR_EM:12626 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-Amelxem1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Amelxem1(IMPC)Ccpcz |
Gene/Transgene symbol | Amelx |
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
- Hypomaturation amelogenesis imperfecta / Orphanet_100033
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal thymus morphology / IMPC
- abnormal lymph node morphology / IMPC
- abnormal tooth morphology / IMPC
- abnormal tooth color / IMPC
- decreased body weight / IMPC
- increased lung tissue damping / IMPC
- enlarged thymus / IMPC
- enlarged stomach / IMPC
- abnormal seminal vesicle morphology / IMPC
- abnormal stomach morphology / IMPC
- abnormal spleen morphology / IMPC
- small spleen / IMPC
- abnormal vertebral arch morphology / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- increased eosinophil cell number / IMPC
- absent teeth / IMPC
- abnormal testis morphology / IMPC
- enlarged lymph nodes / IMPC
- abnormal zygomatic bone morphology / IMPC
- small seminal vesicle / IMPC
- abnormal skin morphology / IMPC
- enlarged heart / IMPC
- decreased lymphocyte cell number / IMPC
- small testis / IMPC
- vertebral transformation / IMPC
- abnormal heart morphology / IMPC
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