Homo sapiens Gene: COG8
Summary
InnateDB Gene IDBG-242959.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol COG8
Gene Name component of oligomeric golgi complex 8
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000213380
Encoded Proteins
component of oligomeric golgi complex 8
component of oligomeric golgi complex 8
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This 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]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:69320140-69339667
Strand Reverse strand
Band q22.1
Transcripts
ENST00000306875 ENSP00000305459
ENST00000564419
ENST00000562595 ENSP00000456705
ENST00000562081 ENSP00000455954
ENST00000567493 ENSP00000464395
ENST00000615447 ENSP00000484442
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 11 experimentally validated interaction(s) in this database.
Experimentally validated
Total 11 [view]
Protein-Protein 11 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0015031 protein transport
Cellular Component
GO:0000139 Golgi membrane
GO:0016020 membrane
GO:0017119 Golgi transport complex
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL H3BQV3 J3QRV3
UniProt Splice Variant
Entrez Gene 84342
UniGene Hs.130849 Hs.606628 Hs.729729 Hs.732992
RefSeq NM_032382
HUGO HGNC:18623
OMIM 606979
CCDS CCDS10876
HPRD 07374
IMGT
EMBL AC026464
GenPept
RNA Seq Atlas 84342