Homo sapiens Gene: GOLGA6B
Summary
InnateDB Gene IDBG-229898.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GOLGA6B
Gene Name golgin A6 family, member B
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000215186
Encoded Proteins
golgin A6 family, member B
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, which are greater than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosomal rearrangements that underlie genomic disease. This gene is a member of the golgin gene family, whose protein products localize to the Golgi apparatus. The majority of the related gene copies are thought to be transcribed pseudogenes. It is not known whether this gene is a pseudogene or if it encodes a golgin protein. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 15:72654738-72666394
Strand Forward strand
Band q24.1
Transcripts
ENST00000421285 ENSP00000408132
ENST00000568532
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [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
Cellular Component
GO:0005794 Golgi apparatus
Orthologs
No orthologs found for this gene
Cross-References
SwissProt A6NDN3
TrEMBL
UniProt Splice Variant
Entrez Gene 55889
UniGene
RefSeq NM_018652
HUGO HGNC:32205
OMIM
CCDS CCDS10245
HPRD
IMGT
EMBL AC009712 AC100827
GenPept
RNA Seq Atlas 55889