FDX2

FDX2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesFDX2, ferredoxin 2, FDX1L, ferredoxin 1 like, MEOAL
External IDsOMIM: 614585; MGI: 1915415; HomoloGene: 31955; GeneCards: FDX2; OMA:FDX2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

112812

68165

Ensembl

ENSG00000267673

ENSMUSG00000079677

UniProt

Q6P4F2

Q9CPW2

RefSeq (mRNA)

NM_080665
NM_001031734
NM_001397406

NM_001039824

RefSeq (protein)

NP_001026904

NP_001034913

Location (UCSC)Chr 19: 10.31 – 10.32 MbChr 9: 21.07 – 21.07 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/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

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000267673 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000079677 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Ferredoxin 2".
  6. ^ 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.

Further reading

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