- 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 |
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:
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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, wild-type C57BL/6N Tac |
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)
Information on how we integrate external resources can be found here
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