Symbol Name ID |
Cubn
cubilin MGI:1931256 |
Darker colors indicate more annotations |
Human Phenotypes | Hydatidiform mole |
Disease(s) Associated with CUBN | |
coronary artery disease |
Mouse Phenotypes | abnormal vitelline vasculature morphology |
failure of initiation of embryo turning |
abnormal endoderm development |
decreased embryo size |
abnormal embryonic tissue morphology |
absent somites |
abnormal allantois morphology |
absent allantois |
absent amnion |
absent chorion |
abnormal vitelline vascular remodeling |
abnormal visceral endoderm morphology |
|
Availability | Mouse Genotype | ||||||||||||
Cubntm1Sarg/Cubntm1Sarg |
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 08/21/2024 MGI 6.24 |
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