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Gene: GOLGA6B (golgin A6 family member B) Homo sapiens
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Symbol: GOLGA6B
Name: golgin A6 family member B
Description: 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]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: GOLGA; GOLGA6D; golgi autoantigen, golgin subfamily a, 6B; golgin A6 family, member B; Golgin subfamily A member 6B; golgin-like protein; putative golgin subfamily A member 6B; Putative golgin subfamily A member 6D
Orthologs:
Pan paniscus (bonobo/pygmy chimpanzee) : LOC100968827 (golgin subfamily A member 6B)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381572,654,697 - 72,667,397 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371572,947,038 - 72,959,738 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361570,734,092 - 70,746,791 (+)NCBINCBI36hg18NCBI36
Build 341570,734,091 - 70,746,791NCBI
Celera1552,501,616 - 52,514,312 (+)NCBI
Cytogenetic Map15q24.1NCBI
HuRef1549,777,633 - 49,790,347 (+)NCBIHuRef
CHM1_11573,065,146 - 73,077,913 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on GOLGA6B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1354461
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-06-18
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.