plasma membrane calcium-transporting ATPase 2 isoform X5 [Homo sapiens - Protein

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De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment. [Hum Genet. 2019]
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment.
Smits JJ, Oostrik J, Beynon AJ, Kant SG, de Koning Gans PAM, Rotteveel LJC, Klein Wassink-Ruiter JS, Free RH, Maas SM, van de Kamp J, et al. Hum Genet. 2019 Jan; 138(1):61-72. Epub 2018 Dec 8.
A V1143F mutation in the neuronal-enriched isoform 2 of the PMCA pump is linked with ataxia. [Neurobiol Dis. 2018]
A V1143F mutation in the neuronal-enriched isoform 2 of the PMCA pump is linked with ataxia.
Vicario M, Zanni G, Vallese F, Santorelli F, Grinzato A, Cieri D, Berto P, Frizzarin M, Lopreiato R, Zonta F, et al. Neurobiol Dis. 2018 Jul; 115:157-166. Epub 2018 Apr 12.
Survival strategies for mouse cerebellar Purkinje neurons lacking PMCA2. [Neurosci Lett. 2018]
Survival strategies for mouse cerebellar Purkinje neurons lacking PMCA2.
Roome CJ, Empson RM. Neurosci Lett. 2018 Jan 10; 663:25-28.

RefSeq genomic sequence
See the genomic reference sequence for the ATP2B2 gene (NG_012046.2).
RefSeq mRNA
See reference mRNA sequence for the ATP2B2 gene (XM_017006488.3).
RefSeq protein isoforms
See 29 reference sequence protein isoforms for the ATP2B2 gene.

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Protein