RecName: Full=Ataxin-7; AltName: Full=Spinocerebellar ataxia type 7 pr - Protein

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Clinical characterization and the improved molecular diagnosis of autosomal dominant cone-rod dystrophy in patients with SCA7. [Mol Vis. 2021]
Clinical characterization and the improved molecular diagnosis of autosomal dominant cone-rod dystrophy in patients with SCA7.
Zou X, Yao F, Li F, Wu S, Li H, Sun Z, Zhu T, Wei X, Li D, Sui R. Mol Vis. 2021; 27:221-232. Epub 2021 May 7.
Deciphering the natural history of SCA7 in children. [Eur J Neurol. 2020]
Deciphering the natural history of SCA7 in children.
Bah MG, Rodriguez D, Cazeneuve C, Mochel F, Devos D, Suppiej A, Roubertie A, Meunier I, Gitiaux C, Curie A, et al. Eur J Neurol. 2020 Nov; 27(11):2267-2276. Epub 2020 Jul 23.
Structural and dynamic studies reveal that the Ala-rich region of ataxin-7 initiates α-helix formation of the polyQ tract but suppresses its aggregation. [Sci Rep. 2019]
Structural and dynamic studies reveal that the Ala-rich region of ataxin-7 initiates α-helix formation of the polyQ tract but suppresses its aggregation.
Hong JY, Wang DD, Xue W, Yue HW, Yang H, Jiang LL, Wang WN, Hu HY. Sci Rep. 2019 May 16; 9(1):7481. Epub 2019 May 16.

RefSeq genomic sequence
See the genomic reference sequence for the ATXN7 gene (NG_008227.1).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the ATXN7 gene.

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O15265 [Domain Mapping of Disease Mut...]
O15265
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Ataxin-7; AltName: Full=Spinocerebellar ataxia type 7 protein
RecName: Full=Ataxin-7; AltName: Full=Spinocerebellar ataxia type 7 protein
gi|5921169|sp|O15265.1|ATX7_HUMAN

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