Symbol Name ID |
B9d1
B9 protein domain 1 MGI:1351471 |
Darker colors indicate more annotations |
Human Phenotypes | Cystic liver disease |
Congenital hepatic fibrosis |
Disease(s) Associated with B9D1 | ||
Meckel syndrome |
Mouse Phenotypes | abnormal bile duct development |
bile duct hyperplasia |
abnormal hepatobiliary system morphology |
abnormal liver morphology |
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Availability | Mouse Genotype | ||||
B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi | |||||
B9d1tm1d(EUCOMM)Wtsi/B9d1tm1d(EUCOMM)Wtsi |
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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