ATP13A2

ATPase type 13A2
Identifiers
Symbols	ATP13A2 ; HSA9947; KRPPD; PARK9
External IDs	Template:OMIM5 Template:MGI HomoloGene: 56940
Gene ontology Molecular function Template:GNF GO Template:GNF GO Template:GNF GO Template:GNF GO Template:GNF GO Template:GNF GO Template:GNF GO Cellular component Template:GNF GO Template:GNF GO Biological process Template:GNF GO Template:GNF GO Template:GNF GO
RNA expression pattern
More reference expression data
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

ATPase type 13A2, also known as ATP13A2, is a human gene.

Further reading

• Hampshire DJ, Roberts E, Crow Y; et al. (2002). "Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36". J. Med. Genet. 38 (10): 680–2. PMID 11584046.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Schultheis PJ, Hagen TT, O'Toole KK; et al. (2004). "Characterization of the P5 subfamily of P-type transport ATPases in mice". Biochem. Biophys. Res. Commun. 323 (3): 731–8. doi:10.1016/j.bbrc.2004.08.156. PMID 15381061.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gregory SG, Barlow KF, McLay KE; et al. (2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. 441 (7091): 315–21. doi:10.1038/nature04727. PMID 16710414.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Ramirez A, Heimbach A, Gründemann J; et al. (2006). "Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase". Nat. Genet. 38 (10): 1184–91. doi:10.1038/ng1884. PMID 16964263.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Di Fonzo A, Chien HF, Socal M; et al. (2007). "ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease". Neurology. 68 (19): 1557–62. doi:10.1212/01.wnl.0000260963.08711.08. PMID 17485642.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)