- increased circulating HDL cholesterol level / IMPC
- abnormal retina blood vessel morphology / IMPC
- increased startle reflex / IMPC
- abnormal retina vasculature morphology / IMPC
- decreased circulating serum albumin level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- abnormal retina morphology / IMPC
- persistence of hyaloid vascular system / IMPC
- increased circulating bilirubin level / IMPC
- abnormal lens morphology / IMPC
- decreased circulating iron level / IMPC
- abnormal vitreous body morphology / IMPC
- decreased blood urea nitrogen level / IMPC
- cataract / IMPC
- increased leukocyte cell number / IMPC
- decreased exploration in new environment / IMPC
- increased circulating cholesterol level / IMPC
- increased circulating unsaturated transferrin level / IMPC
C57BL/6N-Cyp7a1tm1a(EUCOMM)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:09086 |
International strain name | C57BL/6N-Cyp7a1tm1a(EUCOMM)Wtsi/Ieg |
Alternative name | EPD0426_3_C04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cyp7a1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Cyp7a1 |
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 EPD0426_3_C04. 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/6NTacUSA, wild-type C57BL/6NTacUSA |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency / Orphanet_209902
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal liver morphology / MGI
- abnormal liver physiology / MGI
- abnormal skin condition / MGI
- flaky skin / MGI
- oily skin / MGI
- abnormal epidermis stratum basale morphology / MGI
- thin epidermis stratum spinosum / MGI
- abnormal epidermis stratum granulosum morphology / MGI
- hyperkeratosis / MGI
- thin dermal layer / MGI
- delayed eyelid opening / MGI
- hypoactivity / MGI
- decreased exploration in new environment / MGI
- postnatal growth retardation / MGI
- abnormal skin morphology / MGI
- abnormal vision / MGI
- abnormal lipid homeostasis / MGI
- decreased intestinal cholesterol absorption / MGI
- steatorrhea / MGI
- greasy coat / MGI
- dry skin / MGI
- abnormal bile composition / MGI
- abnormal bile salt level / MGI
- abnormal bile salt homeostasis / MGI
- abnormal fat-soluble vitamin level / MGI
- decreased birth weight / MGI
- postnatal lethality, incomplete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
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