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Gene : FOXRED1 Homo sapiens

Name  ? FAD dependent oxidoreductase domain containing 1 Cytological Location  11q24.2
Brief Description  FAD dependent oxidoreductase domain containing 1
Description  This gene encodes a protein that contains a FAD-dependent oxidoreductase domain. The encoded protein is localized to the mitochondria and may function as a chaperone protein required for the function of mitochondrial complex I. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2010]
  • synonyms:
  • HGNC:26927,
  • FOXRED1,
  • uc001qdi.4,
  • FP634,
  • OTTHUMG00000165827,
  • MC1DN19,
  • NM_017547,
  • H17,
  • H17
  • identifiers:
  • 55572,
  • ENSG00000110074,
  • FOXRED1

Genome feature

Region: gene ? Length: 9090  
Location: 11:126269043-126278132 Cyto location: 11q24.2


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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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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

3753 SN Ps

5 Cross References

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results