- hydronephrosis / MGI
- salivary gland epithelial hyperplasia / MGI
- thin skin / MGI
- thin dermal layer / MGI
- abnormal humoral immune response / MGI
- reduced female fertility / MGI
- neoplasm / MGI
- no abnormal phenotype detected / MGI
- decreased susceptibility to bacterial infection / MGI
- tubular nephritis / MGI
- dilated renal tubules / MGI
- decreased skin tensile strength / MGI
- renal interstitial fibrosis / MGI
- abnormal periodontal ligament morphology / MGI
- periodontal ligament hypercellularity / MGI
- abnormal bone structure / MGI
- increased renal tubule apoptosis / MGI
- kidney atrophy / MGI
- homeostasis/metabolism phenotype / MGI
- behavior/neurological phenotype / MGI
- immune system phenotype / MGI
- skeleton phenotype / MGI
- vision/eye phenotype / MGI
- hematopoietic system phenotype / MGI
- loose skin / MGI
- abnormal tendon morphology / MGI
- abnormal cutaneous collagen fibril morphology / MGI
- abnormal renal tubule epithelium morphology / MGI
- abnormal stomach mucosa morphology / MGI
- renal tubule atrophy / MGI
- increased glomerular capsule space / MGI
C57BL/6N-Dcnem1(IMPC)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:11149 |
Citation information | RRID:IMSR_EM:11149 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/6N-Dcnem1(IMPC)Wtsi/WtsiOulu |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Dcnem1(IMPC)Wtsi |
Gene/Transgene symbol | Dcn |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
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 | University of Oulu, Oulu, Finland |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Congenital stromal corneal dystrophy / Orphanet_101068
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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