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Gene : COG7 Homo sapiens

Name  ? component of oligomeric golgi complex 7 Cytological Location  16p12.2
Brief Description  component of oligomeric golgi complex 7
Description  The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010]
  • synonyms:
  • AF070568,
  • CDG2E,
  • uc002dlo.4,
  • OTTHUMG00000094807,
  • COG7,
  • NM_153603,
  • HGNC:18622
  • identifiers:
  • 91949,
  • ENSG00000168434,
  • COG7

Genome feature

Region: gene ? Length: 64723  
Location: 16:23388493-23453215 reverse strand Cyto location: 16p12.2

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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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]


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

Gene Ontology

Gene --> GO terms.



3740 SNPs

5 Cross References

19 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results