• Official Full Name
  • FAD-dependent oxidoreductase domain containing 1
  • Background
  • 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.
  • Synonyms
  • FOXRED1; FAD-dependent oxidoreductase domain containing 1; FAD-dependent oxidoreductase domain-containing protein 1; H17; FAD dependent oxidoreductase domain containing 1; FAD dependent oxidoreductase domain containing protein 1; FOXRED 1; FP634; FXRD1_HUMAN
Source (Host):Wheat GermSpecies:Human
Product nameRecombinant Human FOXRED1 Protein, GST-tagged
Source (Host):E. coliSpecies:Human
Product nameRecombinant Human FOXRED1, His-tagged
Source (Host):Mammalian CellsSpecies:Mouse
Product nameRecombinant Mouse FOXRED1 Protein
Source (Host):Mammalian CellsSpecies:Zebrafish
Product nameRecombinant Zebrafish FOXRED1
Source (Host):Species:Human
Product nameRecombinant Human FOXRED1 293 Cell Lysate

Protein Function

FOXRED1 has several biochemical functions, for example, oxidoreductase activity. Some of the functions are cooperated with other proteins, some of the functions could acted by FOXRED1 itself. We selected most functions FOXRED1 had, and list some proteins which have the same functions with FOXRED1. You can find most of the proteins on our site.
Related Protein
Function oxidoreductase activity
Related Protein DHRS13B; HSD17B12B; CYP2C19; CYP2K22; TDO2A; ALDH9A1A.2; APEX1; CYP2K6; CYP2V1; ETFDH

Interacting Protein

FOXRED1 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with FOXRED1 here. Most of them are supplied by our site. Hope this information will be useful for your research of FOXRED1.

FOXRED1 Related Articles

Saada, A; Edvardson, S; et al. Combined OXPHOS complex I and IV defect, due to mutated complex I assembly factor C20ORF7. JOURNAL OF INHERITED METABOLIC DISEASE 35:125-131(2012).
Alston, CL; He, LP; et al. Maternally inherited mitochondrial DNA disease in consanguineous families. EUROPEAN JOURNAL OF HUMAN GENETICS 19:1226-1229(2011).