- decreased exploration in new environment / IMPC
- abnormal coat appearance / IMPC
- abnormal cholesterol homeostasis / IMPC
- abnormal testis morphology / IMPC
- no spontaneous movement / IMPC
- abnormal heart morphology / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- abnormal coat/ hair morphology / IMPC
- abnormal kidney morphology / IMPC
- small testis / IMPC
- increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number / IMPC
- decreased grip strength / IMPC
- decreased locomotor activity / IMPC
- increased circulating potassium level / IMPC
- small heart / IMPC
- abnormal behavior / IMPC
- abnormal mammary gland morphology / IMPC
- abnormal seminal vesicle morphology / IMPC
- abnormal gallbladder morphology / IMPC
C57BL/6NCrl-Fam83hem2(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:15171 |
Citation information | RRID:IMSR_EM:15171 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-Fam83hem2(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Fam83hem2(IMPC)Ccpcz |
Gene/Transgene symbol | Fam83h |
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
- Hypocalcified amelogenesis imperfecta / Orphanet_100032
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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