- tremors / IMPC
- increased IgE level / IMPC
- decreased circulating free fatty acids level / IMPC
- abnormal bone mineralization / IMPC
- thrombocytopenia / IMPC
- decreased circulating glycerol level / IMPC
- increased mean corpuscular hemoglobin concentration / IMPC
- decreased total body fat amount / IMPC
- decreased grip strength / IMPC
- increased bone mineral content / IMPC
B6Dnk;B6N-Entpd1tm1a(EUCOMM)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:04749 |
International strain name | B6Dnk;B6N-Entpd1tm1a(EUCOMM)Wtsi/Ieg |
Alternative name | EPD0156_1_B01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Entpd1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Entpd1 |
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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0156_1_B01. 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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6Dnk, wild-type C57BL/6Dnk |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive spastic paraplegia type 64 / Orphanet_401810
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased grip strength / IMPC
- decreased circulating glycerol level / IMPC
- increased circulating chloride level / IMPC
- decreased total body fat amount / IMPC
- increased mean corpuscular hemoglobin concentration / IMPC
- increased bone mineral content / IMPC
- thrombocytopenia / IMPC
- tremors / IMPC
- increased IgE level / IMPC
- increased circulating sodium level / IMPC
- abnormal bone mineralization / IMPC
- decreased circulating free fatty acids level / IMPC
MGI phenotypes (gene matching)
- abnormal blood flow velocity / MGI
- impaired smooth muscle contractility / MGI
- abnormal brain morphology / MGI
- abnormal neutrophil physiology / MGI
- increased susceptibility to ischemic brain injury / MGI
- cardiac fibrosis / MGI
- thrombocytopenia / MGI
- liver fibrosis / MGI
- renal fibrosis / MGI
- abnormal vascular endothelial cell physiology / MGI
- abnormal muscle electrophysiology / MGI
- homeostasis/metabolism phenotype / MGI
- hematopoietic system phenotype / MGI
- abnormal neurotransmitter secretion / MGI
- abnormal synaptic norepinephrine release / MGI
- abnormal platelet physiology / MGI
- increased bleeding time / MGI
- pulmonary fibrosis / MGI
- increased cerebral infarction size / MGI
- increased neurotransmitter release / MGI
- decreased platelet aggregation / MGI
- spleen fibrosis / MGI
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