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ONTOLOGY REPORT - ANNOTATIONS


Term:spinocerebellar ataxia type 14
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Accession:DOID:0050964 term browser browse the term
Definition:An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the PRKCG gene. (DO)
Synonyms:exact_synonym: SCA14;   Spinocerebellar Ataxia 14
 primary_id: MESH:C537196;   RDO:0002985
 alt_id: OMIM:605361
For additional species annotation, visit the Alliance of Genome Resources.


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spinocerebellar ataxia type 14 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Prkcg protein kinase C, gamma JBrowse link 1 64,407,098 64,433,698 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15626
    disease of anatomical entity 14956
      nervous system disease 10224
        neurodegenerative disease 2694
          hereditary ataxia 186
            autosomal dominant cerebellar ataxia 63
              spinocerebellar ataxia type 14 1
Path 2
Term Annotations click to browse term
  disease 15626
    disease of anatomical entity 14956
      nervous system disease 10224
        central nervous system disease 8102
          brain disease 7571
            movement disease 1001
              Dyskinesias 711
                Ataxia 302
                  hereditary ataxia 186
                    cerebellar ataxia 169
                      autosomal dominant cerebellar ataxia 63
                        spinocerebellar ataxia type 14 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.