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Symbol
Name
ID
B9d1
B9 protein domain 1
MGI:1351471
Phenotype annotations related to liver/biliary system
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
Availability Mouse Genotype
B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi
B9d1tm1d(EUCOMM)Wtsi/B9d1tm1d(EUCOMM)Wtsi

Contributing Projects:
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
05/14/2024
MGI 6.23
The Jackson Laboratory