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Gene : COG5 Homo sapiens

Name  ? component of oligomeric golgi complex 5 Cytological Location  7q22.3
Brief Description  component of oligomeric golgi complex 5
Description  The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex (COG) required for normal Golgi morphology and function. The encoded protein is organized with conserved oligomeric Golgi complex components 6, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants. Mutations in this gene result in congenital disorder of glycosylation type 2I.[provided by RefSeq, Jan 2011]
  • synonyms:
  • AF058718,
  • CDG2I,
  • OTTHUMG00000023895,
  • GTC90,
  • GOLTC1,
  • golgi transport complex 1 (90 kDa subunit),
  • NM_001161520,
  • uc003vec.3,
  • GOLTC1,
  • GTC90,
  • HGNC:14857,
  • COG5
  • identifiers:
  • 10466,
  • ENSG00000164597,
  • COG5

Genome feature

Region: gene ? Length: 362990  
Location: 7:107201372-107564361 reverse strand Cyto location: 7q22.3


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Function

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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

1 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

3740 SNPs

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results