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ONTOLOGY REPORT - ANNOTATIONS


Term:spinocerebellar ataxia type 6
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Accession:DOID:0050956 term browser browse the term
Definition:An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, has_material_basis_in mutation in the CACNA1A gene. (DO)
Synonyms:exact_synonym: SCA6;   spinocerebellar ataxia 6
 primary_id: RDO:9003727
 alt_id: OMIM:183086
 xref: GARD:10351
For additional species annotation, visit the Alliance of Genome Resources.


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spinocerebellar ataxia type 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cacna1a calcium voltage-gated channel subunit alpha1 A JBrowse link 19 25,453,236 25,749,550 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        neurodegenerative disease 2530
          hereditary ataxia 184
            autosomal dominant cerebellar ataxia 63
              spinocerebellar ataxia type 6 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        central nervous system disease 6931
          brain disease 6435
            movement disease 999
              Dyskinesias 707
                Ataxia 296
                  hereditary ataxia 184
                    cerebellar ataxia 168
                      autosomal dominant cerebellar ataxia 63
                        spinocerebellar ataxia type 6 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.