- 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 |
Citation information | RRID:IMSR_EM:12640 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/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
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).