- abnormal xiphoid process morphology / MGI
- abnormal hair follicle morphology / MGI
- short snout / MGI
- abnormal spermatogenesis / MGI
- thin skin / MGI
- male infertility / MGI
- emphysema / MGI
- no abnormal phenotype detected / MGI
- oligozoospermia / MGI
- abnormal molar morphology / MGI
- abnormal cutaneous collagen fibril morphology / MGI
- triangular face / MGI
C57BL/6NCrl-Adamts2em1(IMPC)Ccpcz/Ph
| Status | Under development - register interest |
| EMMA ID | EM:16648 |
| Citation information | RRID:IMSR_EM:16648 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-Adamts2em1(IMPC)Ccpcz/Ph |
| Alternative name | |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Adamts2em1(IMPC)Ccpcz |
| Gene/Transgene symbol | Adamts2 |
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
- Dermatosparaxis Ehlers-Danlos syndrome / Orphanet_1901
MGI phenotypes (gene matching)
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