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Gene : GOLGA7B Homo sapiens

Name  ? golgin A7 family member B Cytological Location  10q24.2
Brief Description  golgin A7 family member B
  • synonyms:
  • BC008047,
  • chromosome 10 open reading frame 133,
  • bA451M19.3,
  • OTTHUMG00000018869,
  • GOLGA7B,
  • bA451M19.3,
  • HGNC:31668,
  • uc001kos.4,
  • NM_001010917,
  • bA459F3.4,
  • C10orf132,
  • golgi autoantigen, golgin subfamily a, 7B,
  • golgin A7 family, member B,
  • C10orf133,
  • bA459F3.4,
  • C10orf132,
  • chromosome 10 open reading frame 132,
  • C10orf133
  • identifiers:
  • 401647,
  • ENSG00000155265,
  • GOLGA7B

Genome feature

Region: gene ? Length: 21736  
Location: 10:97849843-97871578 Cyto location: 10q24.2


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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

614 SN Ps

5 Cross References

13 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results