Tissue expression
Cell line expression
Protein structure
AC026464.6
Novel protein, COG8-PDF readthroughThis gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008]
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Atlas Antibodies | HPA049429 | Polyclonal |
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Enhanced validation
Supportive data in Antibodypedia
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Data in Antibodypedia (inconclusive)
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Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Recommended by provider