ATP13A2

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ATPase type 13A2
Identifiers
Symbols ATP13A2 ; CLN12; HSA9947; KRPPD; PARK9
External IDs OMIM610513 MGI1922022 HomoloGene56940 GeneCards: ATP13A2 Gene
EC number 3.6.3.8
RNA expression pattern
PBB GE ATP13A2 218608 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 23400 74772
Ensembl ENSG00000159363 ENSMUSG00000036622
UniProt Q9NQ11 Q9CTG6
RefSeq (mRNA) NM_001141973 NM_001164366
RefSeq (protein) NP_001135445 NP_001157838
Location (UCSC) Chr 1:
17.31 – 17.34 Mb
Chr 4:
140.99 – 141.01 Mb
PubMed search [1] [2]

Probable cation-transporting ATPase 13A2 is an enzyme that in humans is encoded by the ATP13A2 gene.[1][2][3]


References[edit]

  1. ^ Schultheis PJ, Hagen TT, O'Toole KK, Tachibana A, Burke CR, McGill DL, Okunade GW, Shull GE (Sep 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. 
  2. ^ Ramirez A, Heimbach A, Grundemann J, Stiller B, Hampshire D, Cid LP, Goebel I, Mubaidin AF, Wriekat AL, Roeper J, Al-Din A, Hillmer AM, Karsak M, Liss B, Woods CG, Behrens MI, Kubisch C (Sep 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. 
  3. ^ "Entrez Gene: ATP13A2 ATPase type 13A2". 

Further reading[edit]