- decreased circulating HDL cholesterol level / IMPC
- increased leukocyte cell number / IMPC
- increased neutrophil cell number / IMPC
- increased monocyte cell number / IMPC
- increased basophil cell number / IMPC
- decreased hemoglobin content / IMPC
- increased circulating alanine transaminase level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased spleen weight / IMPC
- increased lymphocyte cell number / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased circulating bilirubin level / IMPC
- thrombocytosis / IMPC
- increased circulating creatinine level / IMPC
- decreased circulating glucose level / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- increased circulating potassium level / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- increased circulating amylase level / IMPC
- increased red blood cell distribution width / IMPC
C57BL/6NTac-Abcb4em1(IMPC)H/H
Status | Available to order |
EMMA ID | EM:12801 |
Citation information | RRID:IMSR_EM:12801 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-Abcb4em1(IMPC)H/H |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Abcb4em1(IMPC)H |
Gene/Transgene symbol | Abcb4 |
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project 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
- Low phospholipid-associated cholelithiasis / Orphanet_69663
- Progressive familial intrahepatic cholestasis type 3 / Orphanet_79305
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased startle reflex / IMPC
- increased neutrophil cell number / IMPC
- increased spleen weight / IMPC
- increased circulating bilirubin level / IMPC
- increased circulating alanine transaminase level / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- increased red blood cell distribution width / IMPC
- decreased locomotor activity / IMPC
- increased lymphocyte cell number / IMPC
- decreased circulating HDL cholesterol level / IMPC
- increased circulating creatinine level / IMPC
- increased circulating amylase level / IMPC
- increased leukocyte cell number / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased basophil cell number / IMPC
- decreased circulating glucose level / IMPC
- increased monocyte cell number / IMPC
- decreased hemoglobin content / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating potassium level / IMPC
- thrombocytosis / IMPC
- decreased mean corpuscular hemoglobin / IMPC
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