FDX2

FDX2
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2Y5C
Identifiers
Aliases	FDX2, ferredoxin 2, FDX1L, ferredoxin 1 like, MEOAL
External IDs	OMIM: 614585 MGI: 1915415 HomoloGene: 31955 GeneCards: FDX2
Gene location (Human)
Chr.	Chromosome 19 (human)
End	10,316,015 bp
Gene location (Mouse)
Chr.	Chromosome 9 (mouse)
End	21,073,614 bp
RNA expression pattern
	Top expressed in
	prefrontal cortex; ; Brodmann area 9; ; superior frontal gyrus; ; nucleus accumbens; ; hypothalamus; ; substantia nigra; ; temporal lobe; ; hippocampus proper; ; amygdala; ; putamen;
	Top expressed in
	quadriceps femoris muscle; ; white adipose tissue; ; bone marrow; ; muscle tissue; ; proximal tubule; ; skeletal muscle tissue; ; superior frontal gyrus; ; adrenal gland; ; urinary bladder; ; embryo;
	More reference expression data
	n/a
Gene ontology
Molecular function	iron-sulfur cluster binding; protein binding; metal ion binding; 2 iron, 2 sulfur cluster binding; electron transfer activity;
Cellular component	mitochondrial matrix; mitochondrion;
Biological process	C21-steroid hormone biosynthetic process; sterol metabolic process; small molecule metabolic process; electron transport chain;
	Sources:Amigo / QuickGO
Orthologs
	112812
	68165
	ENSG00000267673
	ENSMUSG00000079677
	Q6P4F2
	Q9CPW2
	NM_080665; NM_001031734; NM_001397406
	NM_001039824
	NP_001026904
	NP_001034913
	Wikidata
View/Edit Human	View/Edit Mouse

Ferredoxin 2 is a protein that in humans is encoded by the FDX2 gene. It participates in heme A synthesis and iron-sulphur protein synthesis.^[5]

Mutations in FDX2 cause mitochondrial myopathy.^[6]

References[edit]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000267673 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000079677 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: Ferredoxin 2".
^ Spiegel R, Saada A, Halvardson J, Soiferman D, Shaag A, Edvardson S, Horovitz Y, Khayat M, Shalev SA, Feuk L, Elpeleg O (July 2014). "Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy". European Journal of Human Genetics. 22 (7): 902–6. doi:10.1038/ejhg.2013.269. PMC 4060119. PMID 24281368.