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Symbol
Name
ID

Cog6
component of oligomeric golgi complex 6
MGI:1914792

Phenotype annotations related to nervous system

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
Availability	Mouse Genotype
	Cog6^{tm1a(EUCOMM)Wtsi}/Cog6^{tm1a(EUCOMM)Wtsi}

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23