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Gene : COG4 Homo sapiens

Name  ? component of oligomeric golgi complex 4 Cytological Location  16q22.1
Brief Description  component of oligomeric golgi complex 4
Description  The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2010]
  • synonyms:
  • SWILS,
  • CDG2J,
  • COD1,
  • OTTHUMG00000128515,
  • HGNC:18620,
  • COG4,
  • COD1,
  • NM_001195139,
  • uc002ezc.4,
  • AL050101,
  • DKFZP586E1519
  • identifiers:
  • 25839,
  • ENSG00000103051,
  • COG4

Genome feature

Region: gene ? Length: 42988  
Location: 16:70480567-70523554 reverse strand Cyto location: 16q22.1


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

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Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 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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Expression

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Other

3753 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results