Homo sapiens Gene: COG7
Summary
InnateDB Gene IDBG-20375.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol COG7
Gene Name component of oligomeric golgi complex 7
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000168434
Encoded Proteins
component of oligomeric golgi complex 7
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:23388493-23453180
Strand Reverse strand
Band p12.2
Transcripts
ENST00000307149 ENSP00000305442
ENST00000569635
ENST00000561854 ENSP00000459872
ENST00000563164 ENSP00000460151
ENST00000567821
ENST00000566364
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 23 experimentally validated interaction(s) in this database.
Experimentally validated
Total 23 [view]
Protein-Protein 23 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0006486 protein glycosylation
GO:0006886 intracellular protein transport
GO:0006890 retrograde vesicle-mediated transport, Golgi to ER
GO:0033365 protein localization to organelle
GO:0034067 protein localization to Golgi apparatus
GO:0050821 protein stabilization
Cellular Component
GO:0000139 Golgi membrane
GO:0005794 Golgi apparatus
GO:0017119 Golgi transport complex
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene 91949
UniGene
RefSeq NM_153603 XM_005255681
HUGO HGNC:18622
OMIM 606978
CCDS CCDS10610
HPRD 07373
IMGT
EMBL
GenPept
RNA Seq Atlas 91949