Type | Description |
---|---|
Definition | ataxin 8 |
Date | Results | Publications |
---|---|---|
2018-05-05 10:26:00 | Three SNPs cosegregate with the expanded alleles and spinocerebellar ataxia type 8 in Brazilian family. | 28229454 |
2013-06-15 11:08:00 | suggest that ATXN8 -62 G/A polymorphism plays a role in Taiwanese Parkinson's disease susceptibility | 22577844 |
2013-02-02 11:59:00 | This study identified only one patient with an SCA8 expansion in Greek patients with Huntington's disease. | 22297462 |
2011-12-10 10:51:00 | The spinocerebellar ataxia type 8 is caused by Expansion in ataxin 8 protein. | 21827909 |
2011-11-26 10:35:00 | Report a fluorescent PCR method for detection of expanded repeats in the ATXN8OS/ATXN8 gene in spinocerebellar ataxia type 8. | 22053702 |
Type | IDs |
---|---|
Gene | |
Nucleutide sequences | |
Protein sequencees | |
Others |
UniGene:
Hs.532632,
Hs.645205
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
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Definition: {{{protein.definition}}}Transcript Veriant:{{protein.transcriptVeriant}} Status: {{protein.status}} |
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Location | {{protein.contigId}} ( {{protein.positionStart}}..{{protein.positionEnd}} , {{protein.orientation}} ) | |||||||
Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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