- decreased circulating HDL cholesterol level / IMPC
- decreased circulating glucose level / IMPC
- increased freezing behavior / IMPC
- decreased circulating calcium level / IMPC
- abnormal gait / IMPC
- decreased circulating triglyceride level / IMPC
- abnormal head morphology / IMPC
- impaired cued conditioning behavior / IMPC
- abnormal locomotor behavior / IMPC
- decreased locomotor activity / IMPC
- narrow eye opening / IMPC
- increased circulating iron level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- abnormal startle reflex / IMPC
- increased spleen weight / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased prepulse inhibition / IMPC
- decreased hemoglobin content / IMPC
- increased mean corpuscular hemoglobin / IMPC
- increased monocyte cell number / IMPC
- increased mean corpuscular volume / IMPC
- increased circulating alanine transaminase level / IMPC
- decreased circulating cholesterol level / IMPC
- thrombocytopenia / IMPC
- tremors / IMPC
- decreased erythrocyte cell number / IMPC
- decreased exploration in new environment / IMPC
- increased circulating potassium level / IMPC
- decreased circulating total protein level / IMPC
- abnormal freezing behavior / IMPC
- prolonged RR interval / IMPC
- enlarged spleen / IMPC
- decreased hematocrit / IMPC
- decreased heart rate / IMPC
- increased circulating bilirubin level / IMPC
- abnormal forelimb morphology / IMPC
- decreased startle reflex / IMPC
- decreased circulating serum albumin level / IMPC
- abnormal hindlimb morphology / IMPC
- increased heart weight / IMPC
C57BL/6NTac-Ctsatm2a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:12640 |
International strain name | C57BL/6NTac-Ctsatm2a(EUCOMM)Hmgu/H |
Alternative name | HEPD0507_5_A09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ctsatm2a(EUCOMM)Hmgu |
Gene/Transgene symbol | Ctsa |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0507_5_A09. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Galactosialidosis / Orphanet_351
- Cathepsin A-related arteriopathy-strokes-leukoencephalopathy / Orphanet_575553
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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