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SAMM50

Sorting and assembly machinery component 50 homolog is a protein that in humans is encoded by the SAMM50 gene.[1][2]

Clinical significance

Clinical significance

By means of exome sequencing, two variants – P377A and V231I on the SAMM50 gene were determined to have a potential relationship to the disease phenotype of Ezra,[3] a 3 year old male with neurodevelopmental disorder, episodes of psychomotor regression, history of macrocephaly and history of torticollis. These variants have not been reported previously, making Ezra the only person known to have these variants.

References

References

  1. Humphries AD, Streimann IC, Stojanovski D, Johnston AJ, Yano M, Hoogenraad NJ, Ryan MT (Mar 2005). “Dissection of the mitochondrial import and assembly pathway for human Tom40”. The Journal of Biological Chemistry. 280 (12): 11535–43. doi:10.1074/jbc.M413816200. PMID 15644312.
  2. “Entrez Gene: SAMM50 sorting and assembly machinery component 50 homolog (S. cerevisiae)”.
  3. “describingezra.org – …he looks ridiculously cute in his genes and other important things”. www.describingezra.org. Retrieved 2016-03-07.
Further reading

Further reading

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