Symbol Name ID |
Cyp7b1
cytochrome P450, family 7, subfamily b, polypeptide 1 MGI:104978 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hyperbilirubinemia |
Abnormal circulating cholesterol concentration |
Elevated circulating alanine aminotransferase concentration |
Elevated circulating aspartate aminotransferase concentration |
Elevated circulating alkaline phosphatase concentration |
Abnormality of vitamin metabolism |
Acholic stools |
Disease(s) Associated with CYP7B1 | |||||||
congenital bile acid synthesis defect 3 | |||||||
hereditary spastic paraplegia 5A |
Mouse Phenotypes | homeostasis/metabolism phenotype |
impaired glucose tolerance |
abnormal cholesterol homeostasis |
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Availability | Mouse Genotype | |||
Cyp7b1tm1b(EUCOMM)Wtsi/Cyp7b1tm1b(EUCOMM)Wtsi | ||||
Cyp7b1tm1Rus/Cyp7b1tm1Rus | * |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 09/03/2024 MGI 6.24 |
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