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Gene : GOLGA6B Homo sapiens

Name  ? golgin A6 family member B Cytological Location  15q24.1
Brief Description  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]
  • synonyms:
  • OTTHUMG00000133511,
  • GOLGA6D,
  • uc010uks.2,
  • GOLGA6B,
  • NM_018652,
  • golgin A6 family, member B,
  • GOLGA,
  • golgi autoantigen, golgin subfamily a, 6B,
  • HGNC:32205
  • identifiers:
  • 55889,
  • ENSG00000215186,
  • GOLGA6B

Genome feature

Region: gene ? Length: 12701  
Location: 15:72654697-72667397 Cyto location: 15q24.1


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Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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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

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

480 SN Ps

3 Cross References

12 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results