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ATP13A2, ATPase cation transporting 13A2

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ATP13A2, ATPase cation transporting 13A2

  • This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008]

  • Gene Synonyms (polyamine-transporting ATPase 13A2, cation-transporting ATPase 13A2, ATPase 13A2, ATPase type 13A2, probable cation-transporting ATPase 13A2, CLN12, HSA9947, KRPPD, PARK9, SPG78,)
  • NCBI Gene ID: 23400
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q8NBS1
    UNIPROT ID#>>Q8N4D4
    UNIPROT ID#>>Q9NQ11
  • 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.

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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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