ATP13A2

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ATP13A2
Identifiers
Aliases ATP13A2, CLN12, HSA9947, KRPPD, PARK9, ATPase 13A2
External IDs MGI: 1922022 HomoloGene: 56940 GeneCards: ATP13A2
RNA expression pattern
PBB GE ATP13A2 218608 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001141973
NM_001141974
NM_022089

NM_001164366
NM_029097

RefSeq (protein)

NP_001135445
NP_001135446
NP_071372
NP_001135445.1
NP_001135446.1

NP_083373.2

Location (UCSC) Chr 1: 16.99 – 17.01 Mb Chr 4: 140.99 – 141.01 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Probable cation-transporting ATPase 13A2 is an enzyme that in humans is encoded by the ATP13A2 gene.[3][4][5]

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ Schultheis PJ, Hagen TT, O'Toole KK, Tachibana A, Burke CR, McGill DL, Okunade GW, Shull GE (Oct 2004). "Characterization of the P5 subfamily of P-type transport ATPases in mice". Biochemical and Biophysical Research Communications. 323 (3): 731–8. doi:10.1016/j.bbrc.2004.08.156. PMID 15381061. 
  4. ^ Ramirez A, Heimbach A, Gründemann 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 (Oct 2006). "Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase". Nature Genetics. 38 (10): 1184–91. doi:10.1038/ng1884. PMID 16964263. 
  5. ^ "Entrez Gene: ATP13A2 ATPase type 13A2". 

External links[edit]

Further reading[edit]