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Symbol
Name
ID
Cog5
component of oligomeric golgi complex 5
MGI:2145130
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Abnormality of the frontal hairline
Premature skin wrinkling
Disease(s) Associated with COG5
congenital disorder of glycosylation type IIi

Mouse Phenotypes
abnormal skin morphology
Availability Mouse Genotype
Cog5em1(IMPC)Ccpcz/Cog5+

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
05/14/2024
MGI 6.23
The Jackson Laboratory