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Symbol Name ID |
Cog7
component of oligomeric golgi complex 7 MGI:2685013 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal heart morphology |
Secundum atrial septal defect |
Perimembranous ventricular septal defect |
Congestive heart failure |
Splenomegaly |
Hepatosplenomegaly |
| Disease(s) Associated with COG7 | ||||||
| congenital disorder of glycosylation type IIe |
| Mouse Phenotypes | abnormal sinus arrhythmia |
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| Availability | Mouse Genotype | |
| Cog7tm1b(EUCOMM)Hmgu/Cog7+ | ||
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 05/28/2024 MGI 6.13 |
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