Symbol Name ID |
Cog6
component of oligomeric golgi complex 6 MGI:1914792 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Hydrocephalus |
Ventriculomegaly |
Abnormal cortical gyration |
Hypoplasia of the corpus callosum |
Cerebral atrophy |
Cerebellar atrophy |
Intellectual disability |
Global developmental delay |
Seizure |
Disease(s) Associated with COG6 | ||||||||||
congenital disorder of glycosylation type IIl |
Mouse Phenotypes | intracerebral hemorrhage |
thin hypoglossal nerve |
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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 05/14/2024 MGI 6.23 |
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