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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ATP13A2-20-RE | 20 (40 μL) | 200 μL |  |
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| ATP13A2-20-OR | 20 (40 μL) | 200 μL |  |
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| ATP13A2-20-GO | 20 (40 μL) | 200 μL |  |
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| ATP13A2-20-GR | 20 (40 μL) | 200 μL |  |
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| ATP13A2-20-AQ | 20 (40 μL) | 200 μL |  |
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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 Symbol : ATP13A2
Gene Name : ATPase 13A2
Chromosome : CHR 1: 170,119,71-169,859,57
Locus : 1p36.13
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