- absent mandible / MGI
- microcephaly / MGI
- abnormal forelimb morphology / MGI
- abnormal hindlimb morphology / MGI
- polydactyly / MGI
- syndactyly / MGI
- ectopic digits / MGI
- abnormal telencephalon morphology / MGI
- anophthalmia / MGI
- thick apical ectodermal ridge / MGI
- abnormal craniofacial development / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- small interparietal bone / MGI
- small parietal bone / MGI
- absent nasal bone / MGI
- absent maxilla / MGI
- abnormal limb bud morphology / MGI
- absent nasal placodes / MGI
- absent optic vesicle / MGI
- abnormal first pharyngeal arch morphology / MGI
- abnormal mandibular prominence morphology / MGI
- neonatal lethality, complete penetrance / MGI
- decreased midbrain size / MGI
- decreased forebrain size / MGI
- rostral body truncation / MGI
- absent frontonasal prominence / MGI
- absent diencephalon / MGI
- abnormal anterior head development / MGI
C57BL/6NCrl-Dkk1em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:14824 |
Citation information | RRID:IMSR_EM:14824 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-Dkk1em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Dkk1em1(IMPC)Ccpcz |
Gene/Transgene symbol | Dkk1 |
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
- Arnold-Chiari malformation type I / Orphanet_268882
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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