- abnormal sinus arrhythmia / IMPC
- increased heart rate variability / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal skin morphology / IMPC
- decreased exploration in new environment / IMPC
- limb grasping / IMPC
- decreased lymphocyte cell number / IMPC
- increased neutrophil cell number / IMPC
- abnormal gait / IMPC
- decreased circulating serum albumin level / IMPC
- increased mean corpuscular hemoglobin / IMPC
- cardiovascular system phenotype / IMPC
- increased circulating triglyceride level / IMPC
- decreased monocyte cell number / IMPC
- abnormal heart morphology / IMPC
- persistence of hyaloid vascular system / IMPC
- cataract / IMPC
C57BL/6N-Atn1tm1a(EUCOMM)Wtsi/Cnrm
Status | Available to order |
EMMA ID | EM:04826 |
Citation information | RRID:IMSR_EM:04826 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-Atn1tm1a(EUCOMM)Wtsi/Cnrm |
Alternative name | EPD0289_1_F08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Atn1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Atn1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | CNR, Consiglio Nazionale delle Ricerche |
Provider affiliation | EMMA-Monterotondo Campus International Development, CNR, Consiglio Nazionale delle Ricerche |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0289_1_F08. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Animals used for archiving | heterozygous C57BL/6NTac males, wild-type C57BL/6NTac females |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Dentatorubral pallidoluysian atrophy / Orphanet_101
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)