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AFG3L2

Official Full Name
AFG3 like matrix AAA peptidase subunit 2
Organism
Homo sapiens
GeneID
10939
Background
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. [provided by RefSeq, Jul 2008]
Synonyms
OPA12; SCA28; SPAX5;

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