- increased body weight / IMPC
- abnormal tail movements / IMPC
- abnormal coat/hair pigmentation / IMPC
- decreased mean corpuscular volume / IMPC
- increased blood urea nitrogen level / IMPC
- decreased circulating amylase level / IMPC
- increased total body fat amount / IMPC
- decreased circulating magnesium level / IMPC
C57BL/6NTac-Ppp3catm2e(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:05704 |
International strain name | C57BL/6NTac-Ppp3catm2e(EUCOMM)Wtsi/WtsiBiat |
Alternative name | EPD0200_3_B01 |
Strain type | Targeted Mutant Strains : Targeted Non-conditional |
Allele/Transgene symbol | Ppp3catm2e(EUCOMM)Wtsi |
Gene/Transgene symbol | Ppp3ca |
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 EUCOMM ES clone EPD0200_3_B01. For further details on the construction of this clone see the page at the IMPC portal. The targeted allele has lost the 3' loxP site. These mutations cannot be converted into conditional alleles. Click here for more information on EUCOMM final vectors. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | University of Veterinary Medicine, Vienna, Austria |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal dominant non-syndromic intellectual disability / Orphanet_178469
- Undetermined early-onset epileptic encephalopathy / Orphanet_442835
- Craniosynostosis-microretrognathia-severe intellectual disability syndrome / Orphanet_565858
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased circulating magnesium level / IMPC
- increased body weight / IMPC
- increased blood urea nitrogen level / IMPC
- decreased circulating amylase level / IMPC
- decreased mean corpuscular volume / IMPC
- abnormal tail movements / IMPC
- increased total body fat amount / IMPC
- abnormal coat/hair pigmentation / IMPC
MGI phenotypes (gene matching)
- decreased circulating calcium level / MGI
- decreased body weight / MGI
- premature death / MGI
- abnormal hippocampal mossy fiber morphology / MGI
- abnormal urine osmolality / MGI
- decreased urine osmolality / MGI
- decreased T cell proliferation / MGI
- increased circulating creatinine level / MGI
- decreased circulating glucose level / MGI
- increased blood urea nitrogen level / MGI
- decreased interferon-gamma secretion / MGI
- decreased interleukin-2 secretion / MGI
- decreased interleukin-4 secretion / MGI
- increased skeletal muscle fiber diameter / MGI
- decreased skeletal muscle fiber number / MGI
- abnormal skeletal muscle fiber type ratio / MGI
- decreased urine creatinine level / MGI
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