Symbol Name ID |
Cog6
component of oligomeric golgi complex 6 MGI:1914792 |
Darker colors indicate more annotations |
Human Phenotypes | Atrial septal defect |
Ventricular septal defect |
Patent ductus arteriosus |
Splenomegaly |
Disease(s) Associated with COG6 | ||||
congenital disorder of glycosylation type IIl |
Mouse Phenotypes | abnormal vertebral artery topology |
abnormal liver vasculature morphology |
abnormal vitelline vein connection |
abnormal ductus venosus valve morphology |
abnormal inferior vena cava morphology |
dual inferior vena cava |
abnormal coronary sinus connection |
abnormal inferior vena cava valve morphology |
muscular ventricular septal defect |
intracerebral hemorrhage |
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Availability | Mouse Genotype | ||||||||||
Cog6tm1a(EUCOMM)Wtsi/Cog6tm1a(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 04/16/2024 MGI 6.23 |
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