FDX1L

Available structures

Ortholog search: PDBe RCSB

List of PDB id codes
2Y5C

Identifiers

FDX1L, FDX2, ferredoxin 1 like

External IDs

Gene ontology
Molecular function	• iron-sulfur cluster binding • protein binding • metal ion binding • 2 iron, 2 sulfur cluster binding • electron carrier activity
Cellular component	• mitochondrial matrix • mitochondrion
Biological process	• C21-steroid hormone biosynthetic process • sterol metabolic process • oxidation-reduction process • small molecule metabolic process
Sources:Amigo / QuickGO

Orthologs

Species

Human

Mouse

Entrez


112812


68165


ENSG00000267673


ENSMUSG00000079677


Q6P4F2


Q9CPW2

RefSeq (mRNA)


NM_080665 NM_001031734


NM_001039824

RefSeq (protein)


NP_001026904


NP_001034913

Location (UCSC)

PubMed search

^[1]

^[2]

Ferredoxin 1-like is a protein that in humans is encoded by the FDX1L gene.^[3]

Mutations in FDX1L cause mitochondrial myopathy .^[4]

References

↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ "Entrez Gene: Ferredoxin 1-like".
↑ 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. PMID 24281368. doi:10.1038/ejhg.2013.269.