功能： disease:Defects in ATXN10 are the cause of spinocerebellar ataxia type 10 (SCA10) [MIM:603516]. Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA10 is an autosomal dominant cerebellar ataxia (ADCA).,similarity:Belongs to the ataxin-10 family.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasm, perinuclear region .
组织表达： Expressed in the central nervous system.
科研货号： PLA006322
ATX10 Polyclonal Antibody
Catalog NoPLA006322
Product information
基因名称： ATXN10 SCA10
蛋白名称： Ataxin-10 (Brain protein E46 homolog) (Spinocerebellar ataxia type 10 protein)
功能： disease:Defects in ATXN10 are the cause of spinocerebellar ataxia type 10 (SCA10) [MIM:603516]. Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA10 is an autosomal dominant cerebellar ataxia (ADCA).,similarity:Belongs to the ataxin-10 family.,
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