- abnormal lung morphology / IMPC
- decreased locomotor activity / IMPC
- decreased circulating triglyceride level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased circulating bilirubin level / IMPC
- increased circulating amylase level / IMPC
- increased circulating fructosamine level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- increased circulating unsaturated transferrin level / IMPC
C57BL/6N-Abcb11tm1b(EUCOMM)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:08089 |
International strain name | C57BL/6N-Abcb11tm1b(EUCOMM)Hmgu/Ieg |
Alternative name | HEPD0507_7_B05 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Abcb11tm1b(EUCOMM)Hmgu |
Gene/Transgene symbol | Abcb11 |
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 HEPD0507_7_B05. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele (Gt(ROSA)26Sor |
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/6NTacUSA, wild-type C57BL/6NTacUSA |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Progressive familial intrahepatic cholestasis type 2 / Orphanet_79304
- Benign recurrent intrahepatic cholestasis type 2 / Orphanet_99961
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased circulating amylase level / IMPC
- abnormal retina morphology / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating potassium level / IMPC
- abnormal lung morphology / IMPC
- increased circulating unsaturated transferrin level / IMPC
- decreased locomotor activity / IMPC
- decreased circulating triglyceride level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- increased circulating fructosamine level / IMPC
- increased lean body mass / IMPC
- increased circulating bilirubin level / IMPC
MGI phenotypes (gene matching)
- enlarged liver / MGI
- abnormal hepatocyte morphology / MGI
- decreased body weight / MGI
- postnatal growth retardation / MGI
- increased cholesterol level / MGI
- abnormal bile secretion / MGI
- abnormal bile salt level / MGI
- abnormal phospholipid level / MGI
- increased bile salt level / MGI
- intrahepatic cholestasis / MGI
- decreased glycogen level / MGI
- abnormal bile canaliculus morphology / MGI
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