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Gene : COA6 Homo sapiens

Name  ? cytochrome c oxidase assembly factor 6 Cytological Location  1q42.2
Brief Description  cytochrome c oxidase assembly factor 6
Description  This gene encodes a member of the cytochrome c oxidase subunit 6B family. The encoded protein associates with cytochrome c oxidase may act has an cytochrome c oxidase mitochondrial respiratory complex VI assembly factor. Mutations in this gene may be associated with fatal infantile cardiomyopathy. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]
  • synonyms:
  • NM_001012985,
  • CEMCOX4,
  • C1orf31,
  • uc057qls.1,
  • cytochrome c oxidase assembly factor 6 homolog (S. cerevisiae),
  • chromosome 1 open reading frame 31,
  • HGNC:18025,
  • C1orf31,
  • OTTHUMG00000037945,
  • COA6,
  • MC4DN13
  • identifiers:
  • 388753,
  • ENSG00000168275,
  • COA6

Genome feature

Region: gene ? Length: 11625  
Location: 1:234373456-234385080 Cyto location: 1q42.2


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Function

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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

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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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

3740 SNPs

5 Cross References

16 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results