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Symbol
Name
ID
Cog6
component of oligomeric golgi complex 6
MGI:1914792
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Retrognathia
Microcephaly
Enamel hypoplasia
Postaxial polydactyly
Hip dysplasia
Disease(s) Associated with COG6
congenital disorder of glycosylation type IIl

Mouse Phenotypes
fusion of vertebral arches
vertebral transformation
abnormal bone structure
decreased bone mineral content
Availability Mouse Genotype
Cog6tm1a(EUCOMM)Wtsi/Cog6tm1a(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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory