C57BL/6NTac-Ppp2r2btm1a(KOMP)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:14001 |
International strain name | C57BL/6NTac-Ppp2r2btm1a(KOMP)Wtsi/WtsiOulu |
Alternative name | EPD0150_1_D07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ppp2r2btm1a(KOMP)Wtsi |
Gene/Transgene symbol | Ppp2r2b |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0150_1_D07. 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 | University of Oulu, Oulu, Finland |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Spinocerebellar ataxia type 12 / Orphanet_98762
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased leukocyte cell number / IMPC
- hyperactivity / IMPC
- increased circulating creatine kinase level / IMPC
- increased monocyte cell number / IMPC
- abnormal cholesterol homeostasis / IMPC
- thrombocytopenia / IMPC
- abnormal retina morphology / IMPC
- increased fasting circulating glucose level / IMPC
- decreased heart rate variability / IMPC
- decreased mean corpuscular hemoglobin / IMPC
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