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GENE - TERM ANNOTATION REPORT

22 Annotations Found.

An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by OMIM:613647
  • Original References(s): PMID:24833714


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:25741868 PMID:32860008


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:24833714 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:28492532 PMID:28832565


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:25333062 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:25741868


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:26085577


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:20613862


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:24926664 PMID:26467025 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:24482476


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:20613862 PMID:27606357 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:26467025


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:25741868 PMID:27606357 PMID:28492532


  • An association has been curated linking Ap5z1 and hereditary spastic paraplegia 48 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 AP5Z1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 5 papers in RGD have been used to annotate Ap5z1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 48, autosomal recessive
  • Original References(s): PMID:26467025 PMID:28492532 PMID:28832565


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