RecName: Full=V-type proton ATPase catalytic subunit A; Short=V-ATPase - Protein

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Expanding the Spectrum of Autosomal Dominant ATP6V1A-Related Disease: Case Report and Literature Review. [Genes (Basel). 2024]
Expanding the Spectrum of Autosomal Dominant ATP6V1A-Related Disease: Case Report and Literature Review.
Sirchia F, Taietti I, Donesana M, Bassanese F, Clemente AM, Barbato E, Orsini A, Ferretti A, Marseglia GL, Savasta S, et al. Genes (Basel). 2024 Sep 18; 15(9). Epub 2024 Sep 18.
ATP6V1A variants are associated with childhood epilepsy with favorable outcome. [Seizure. 2024]
ATP6V1A variants are associated with childhood epilepsy with favorable outcome.
Li B, Lan S, Liu XR, Ji JJ, He YY, Zhang DM, Xu J, Sun H, Shi Z, Wang J, et al. Seizure. 2024 Mar; 116:81-86. Epub 2023 Aug 9.
Rare human ATP6V1A variants provide unique insights into V-ATPase functions. [Brain. 2022]
Rare human ATP6V1A variants provide unique insights into V-ATPase functions.
Groszer M. Brain. 2022 Aug 27; 145(8):2626-2628.

RefSeq genomic sequence
See the genomic reference sequence for the ATP6V1A gene (NG_047012.1).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the ATP6V1A gene.

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P38606 [Domain Mapping of Disease Mut...]
P38606
Domain Mapping of Disease Mutations
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
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Protein