Symbol Name ID |
B9d1
B9 protein domain 1 MGI:1351471 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal cardiovascular system morphology |
Situs inversus totalis |
Asplenia |
Accessory spleen |
Disease(s) Associated with B9D1 | ||||
Meckel syndrome |
Mouse Phenotypes | abnormal cardiovascular system morphology |
abnormal blood vessel morphology |
thin myocardium |
dextrocardia |
ventricular septal defect |
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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 08/02/2024 MGI 6.24 |
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