AFG3L2( Human )

Entrez Gene 10939 Entrez Gene 10939
AFG3 like matrix AAA peptidase subunit 2

Alias

SCA28|SPAX5

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].

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