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Spinocerebellar ataxia type 7 (SCA7) belongs to a class of hereditary neurodegenrative diseases characterized by abnormally expanded polyglutamine (CAG) repeats at the N-terminus. This autosomal dominant cerebellar ataxia primarily affects the cerebellum, retina, and brain stem and causes dementia, macular degeneration and other neurodegenerative characteristics. SCA7 gene encodes the ubiquitous 892 residue protein ataxin-7. This protein is typically located in the cytoplasm and on the nuclear membrane of normal brain neurons. In cells where there is a mutation of the SCA7 gene, ataxin 7 accumulates in intranuclear inclusions and can result in cell death.
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Protein Aliases: ataxin 7; Ataxin-7; spinocerebellar ataxia 7 homolog; Spinocerebellar ataxia type 7 protein; Spinocerebellar ataxia type 7 protein homolog
Gene Aliases: A430107N12Rik; ADCAII; AI627028; ataxin-7; ATXN7; OPCA3; RGD1562692; SCA7
UniProt ID: (Human) O15265, (Mouse) Q8R4I1
Entrez Gene ID: (Human) 6314, (Mouse) 246103, (Rat) 361015
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