Suvarna Garge (Editor)

AFG3L2

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Species
  
Human

Entrez
  
10939

Human
  
Mouse

Ensembl
  
ENSG00000141385

Aliases
  
AFG3L2, SCA28, SPAX5, AFG3 like matrix AAA peptidase subunit 2

External IDs
  
MGI: 1916847 HomoloGene: 4947 GeneCards: AFG3L2

AFG3 ATPase family gene 3-like 2 (S. cerevisiae) is a protein that in humans is encoded by the AFG3L2 gene.

This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders as well as spastic ataxia-neuropathy syndrome.

References

AFG3L2 Wikipedia