Symbol Name ID |
Cog5
component of oligomeric golgi complex 5 MGI:2145130 |
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 |
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Availability | Mouse Genotype | |
Cog5em1(IMPC)Ccpcz/Cog5+ |
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 12/17/2024 MGI 6.24 |
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