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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:40886526 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:25741868


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:13528413 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:25741868 PMID:30420557


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:14349830 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:30420557


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:14349839 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:30420557


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:13528411 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:25741868 PMID:30420557


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:14349842 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:30420557


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:14349834 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:30420557


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:14349837 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:25741868 PMID:30420557


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:40815678 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:25741868


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:40815679 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
  • Original References(s): PMID:25741868


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:126744923 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: Neurodegeneration, childhood-onset, with cerebellar atrophy
  • Original References(s): PMID:25741868


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:126744916 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: Neurodegeneration, childhood-onset, with cerebellar atrophy
  • Original References(s): PMID:25741868


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:14349832 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: Neurodegeneration, childhood-onset, with cerebellar atrophy
  • Original References(s): PMID:25741868 PMID:30420557 PMID:33624935


  • An association has been curated linking AGTPBP1 and Childhood-Onset Neurodegeneration with Cerebellar Atrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:126744927 (Homo sapiens)
  • 1 RGD objects have been annotated to Childhood-Onset Neurodegeneration with Cerebellar Atrophy  (DOID:9000084)
  • 2 papers in RGD have been used to annotate AGTPBP1
  • Curation Notes: ClinVar Annotator: match by term: Neurodegeneration, childhood-onset, with cerebellar atrophy
  • Original References(s): PMID:25741868


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