ISCU

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Identifiers
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External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
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Iron-sulfur cluster assembly enzyme ISCU, mitochondrial is a protein that in humans is encoded by the ISCU gene.[1][2][3]

A deficiency of ISCU is associated with a mitochondrial myopathy with lifelong exercise intolerance where only minor exertion causes tachycardia, shortness of breath, muscle weakness and myalgia.[4]

References

  1. Hwang DM, Dempsey A, Tan KT, Liew CC (Nov 1996). "A modular domain of NifU, a nitrogen fixation cluster protein, is highly conserved in evolution". Journal of Molecular Evolution. 43 (5): 536–40. doi:10.1007/BF02337525. PMID 8875867.
  2. Tong WH, Rouault T (Nov 2000). "Distinct iron-sulfur cluster assembly complexes exist in the cytosol and mitochondria of human cells". The EMBO Journal. 19 (21): 5692–700. doi:10.1093/emboj/19.21.5692. PMC 305809. PMID 11060020.
  3. "Entrez Gene: ISCU iron-sulfur cluster scaffold homolog (E. coli)".
  4. Mochel F, Haller RG (2009-03-31). "Myopathy with Deficiency of ISCU". GeneReviews. Updated 2011 Sep 1

Further reading

External links