ATP1A2 Gene

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Zhou, V. ATP1A2 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4793 (accessed on 28 September 2026).

Zhou V. ATP1A2 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4793. Accessed September 28, 2026.

Zhou, Vicky. "ATP1A2 Gene" Encyclopedia, https://encyclopedia.pub/entry/4793 (accessed September 28, 2026).

Zhou, V. (2020, December 24). ATP1A2 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4793

Zhou, Vicky. "ATP1A2 Gene." Encyclopedia. Web. 24 December, 2020.

ATP1A2 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/atp1a2

ATPase Na+/K+ transporting subunit alpha 2

genes

References

Bassi MT, Bresolin N, Tonelli A, Nazos K, Crippa F, Baschirotto C, Zucca C,Bersano A, Dolcetta D, Boneschi FM, Barone V, Casari G. A novel mutation in theATP1A2 gene causes alternating hemiplegia of childhood. J Med Genet. 2004Aug;41(8):621-8.
Castro MJ, Nunes B, de Vries B, Lemos C, Vanmolkot KR, van den Heuvel JJ,Temudo T, Barros J, Sequeiros J, Frants RR, Koenderink JB, Pereira-Monteiro JM,van den Maagdenberg AM. Two novel functional mutations in the Na+,K+-ATPasealpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine andassociated neurological phenotypes. Clin Genet. 2008 Jan;73(1):37-43.
de Vries B, Freilinger T, Vanmolkot KR, Koenderink JB, Stam AH, Terwindt GM,Babini E, van den Boogerd EH, van den Heuvel JJ, Frants RR, Haan J, Pusch M, van den Maagdenberg AM, Ferrari MD, Dichgans M. Systematic analysis of three FHMgenes in 39 sporadic patients with hemiplegic migraine. Neurology. 2007 Dec4;69(23):2170-6.
Jurkat-Rott K, Freilinger T, Dreier JP, Herzog J, Göbel H, Petzold GC,Montagna P, Gasser T, Lehmann-Horn F, Dichgans M. Variability of familialhemiplegic migraine with novel A1A2 Na+/K+-ATPase variants. Neurology. 2004 May25;62(10):1857-61.
Pietrobon D. Familial hemiplegic migraine. Neurotherapeutics. 2007Apr;4(2):274-84. Review.
Riant F, De Fusco M, Aridon P, Ducros A, Ploton C, Marchelli F, Maciazek J,Bousser MG, Casari G, Tournier-Lasserve E. ATP1A2 mutations in 11 families withfamilial hemiplegic migraine. Hum Mutat. 2005 Sep;26(3):281.
Riant F, Ducros A, Ploton C, Barbance C, Depienne C, Tournier-Lasserve E. Denovo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadichemiplegic migraine. Neurology. 2010 Sep 14;75(11):967-72. doi:10.1212/WNL.0b013e3181f25e8f.
Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE, Leppert MF,Schlesinger-Massart MB, Ptacek LJ, Silver K, Youroukos S. Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation. AnnNeurol. 2004 Jun;55(6):884-7.
Tavraz NN, Dürr KL, Koenderink JB, Freilinger T, Bamberg E, Dichgans M,Friedrich T. Impaired plasma membrane targeting or protein stability by certainATP1A2 mutations identified in sporadic or familial hemiplegic migraine. Channels(Austin). 2009 Mar-Apr;3(2):82-7.

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Subjects: Genetics & Heredity

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Update Date: 24 Dec 2020

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