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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


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