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ATP13A2

ATPase type 13A2

ATP13A2 belongs to the P-type superfamily of ATPases that transport inorganic cations and other substrates across cell membranes. ATP13A2 has predominantly neuronal expression and transiently transfected cells studies have shown that it is located in lysosomes. Recently a loss-of-function mutation in ATP13A2 has been linked to an autosomal recessive form of early-onset parkinsonism with pyramidal degeneration and dementia.

Gene Name: ATPase type 13A2
Family/Subfamily: Transporter , ATPase - P type, type V
Synonyms: ATP13A2, HSA9947, PARK9, RP1-37C10.4, Putative ATPase, ATPase type 13A2, CLN12, KRPPD
Target Sequences: NM_022089 NP_071372.1 Q9NQ11

Publications (1)

1
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration. Dehay B, Ramirez A, Martinez-Vicente M, Perier C, Canron MH, Doudnikoff E, Vital A, Vila M, Klein C, Bezard E. Proceedings of the National Academy of Sciences of the United States of America. 2012 109:9611-6. (IHC, WB; Human) [PubMed:22647602] [PMC:PMC3386132]

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0.78 - 50 ng/ml
Colorimetric - 450nm (TMB)
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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).