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Gene : CYCS Homo sapiens

Name  ? cytochrome c, somatic Cytological Location  7p15.3
Brief Description  cytochrome c, somatic
Description  This gene encodes a small heme protein that functions as a central component of the electron transport chain in mitochondria. The encoded protein associates with the inner membrane of the mitochondrion where it accepts electrons from cytochrome b and transfers them to the cytochrome oxidase complex. This protein is also involved in initiation of apoptosis. Mutations in this gene are associated with autosomal dominant nonsyndromic thrombocytopenia. Numerous processed pseudogenes of this gene are found throughout the human genome.[provided by RefSeq, Jul 2010]
  • synonyms:
  • HCS,
  • CYC,
  • uc003sxl.4,
  • CYCS,
  • M22877,
  • HGNC:19986,
  • OTTHUMG00000128495,
  • HCS,
  • NM_018947,
  • THC4,
  • CYC
  • identifiers:
  • 54205,
  • ENSG00000172115,
  • CYCS

Genome feature

Region: gene ? Length: 6605  
Location: 7:25118656-25125260 reverse strand Cyto location: 7p15.3


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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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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

263 SN Ps

5 Cross References

19 Data Sets

9 Homologues

0 Located Features

97 Rna Seq Results