Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

43 Annotations Found.

An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia-ocular apraxia-2
  • Original References(s): PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:26467025


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by OMIM:606002
  • Original References(s): PMID:15732101 PMID:17159128


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by OMIM:606002
  • Original References(s): PMID:18414213 PMID:24088041 PMID:26633545


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by OMIM:606002
  • Original References(s): PMID:14770181


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by OMIM:606002
  • Original References(s): PMID:18625865


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by OMIM:606002
  • Original References(s): PMID:17159128


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by OMIM:606002
  • Original References(s): PMID:23806086 PMID:24088041 PMID:26257172


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:25741868 PMID:26467025


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28130640 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:28492532 PMID:29650794


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:19569000 PMID:23129421 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:25174650 PMID:25382069 PMID:26467025 PMID:27013921 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:25741868


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:23757202 PMID:25741868


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:14770181 PMID:25741868 PMID:26467025


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia autosomal recessive 1
  • Original References(s): PMID:25326635 PMID:25741868


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:25025039 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:25741868 PMID:32165824


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:14770181 PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:25382069 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:25025039 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:28642336 PMID:28832565


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:21190393 PMID:22088787 PMID:23129421 PMID:25382069 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia autosomal recessive 1
  • Original References(s): PMID:25741868 PMID:25802885


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:17159128 PMID:19569000 PMID:20981092 PMID:23941260 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:19696032 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Ataxia with Oculomotor Apraxia
  • Original References(s): PMID:19696032 PMID:22088787 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:26601740 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:19569000 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:23129421 PMID:25741868 PMID:26467025 PMID:28492532 PMID:28642336


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:19569000 PMID:23129421


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:20540686 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:25299611 PMID:26467025 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:25802885 PMID:28492532


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:18058631 PMID:23129421 PMID:23881933 PMID:26467025 PMID:27790088 PMID:28492532 PMID:28832565


  • An association has been curated linking Setx and ataxia with oculomotor apraxia type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SETX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to ataxia with oculomotor apraxia type 2  (DOID:0050755)
  • 5 papers in RGD have been used to annotate Setx
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
  • Original References(s): PMID:23881933 PMID:25741868 PMID:26467025 PMID:28492532


  • Go Back to source page   Continue to Ontology report