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SPG7, SPG7 matrix AAA peptidase subunit, paraplegin

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SPG7, SPG7 matrix AAA peptidase subunit, paraplegin

  • This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2014]

  • Gene Synonyms (paraplegin, SPG7, paraplegin matrix AAA peptidase subunit, cell matrix adhesion regulator, spastic paraplegia 7 (pure and complicated autosomal recessive), spastic paraplegia 7 protein, CAR, CMAR, PGN, SPG5C,)
  • NCBI Gene ID: 6687
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9UQ90
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

SPG7 matrix AAA peptidase subunit, paraplegin interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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