help  | about  | cite  | software

Gene : GOLGA6A Homo sapiens

Name  ? golgin A6 family member A Cytological Location  15q24.1
Brief Description  golgin A6 family member A
Description  The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The protein encoded by this gene is a member of the golgin family of proteins, whose members localize to the Golgi. This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, that are greather than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosome rearrangements that underlie genomic disease. The protein encoded by this gene is thought to be a functional golgin protein while the majority of the related copies of this gene are thought to be transcribed pseudogenes. [provided by RefSeq, Jul 2008]
  • synonyms:
  • GOLGA6,
  • AF263742,
  • golgi autoantigen, golgin subfamily a, 6A,
  • GLP,
  • GLP,
  • golgi autoantigen, golgin subfamily a, member 6,
  • NM_001038640,
  • uc002axa.1,
  • OTTHUMG00000173035,
  • GOLGA6A,
  • golgi autoantigen, golgin subfamily a, 6,
  • golgin A6 family, member A,
  • GOLGA6,
  • HGNC:13567
  • identifiers:
  • 342096,
  • ENSG00000159289,
  • GOLGA6A

Genome feature

Region: gene ? Length: 12694  
Location: 15:74069857-74082550 reverse strand Cyto location: 15q24.1


Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer

Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

Homologue Displayer

Interactions

Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

47 SN Ps

5 Cross References

14 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results