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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking Fbxo38 and distal hereditary motor neuronopathy type 2D 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 FBXO38 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 2D  (DOID:0111210)
  • 4 papers in RGD have been used to annotate Fbxo38


    • An association has been curated linking Fbxo38 and distal hereditary motor neuronopathy type 2D 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 FBXO38 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 2D  (DOID:0111210)
  • 4 papers in RGD have been used to annotate Fbxo38
  • Curation Notes: ClinVar Annotator: match by term: SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT
  • Original References(s): PMID:28492532


    • An association has been curated linking Fbxo38 and distal hereditary motor neuronopathy type 2D 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 FBXO38 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 2D  (DOID:0111210)
  • 4 papers in RGD have been used to annotate Fbxo38
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy 2D
  • Original References(s): PMID:24207122 PMID:28492532


    • An association has been curated linking Fbxo38 and distal hereditary motor neuronopathy type 2D 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 FBXO38 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 2D  (DOID:0111210)
  • 4 papers in RGD have been used to annotate Fbxo38
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy 2D
  • Original References(s): PMID:24207122 PMID:28492532 PMID:7723957


    • An association has been curated linking Fbxo38 and distal hereditary motor neuronopathy type 2D 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 FBXO38 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 2D  (DOID:0111210)
  • 4 papers in RGD have been used to annotate Fbxo38
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy 2D


    • An association has been curated linking Fbxo38 and distal hereditary motor neuronopathy type 2D 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 FBXO38 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 2D  (DOID:0111210)
  • 4 papers in RGD have been used to annotate Fbxo38
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy 2D
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking Fbxo38 and distal hereditary motor neuronopathy type 2D 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 FBXO38 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 2D  (DOID:0111210)
  • 4 papers in RGD have been used to annotate Fbxo38
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy 2D
  • Original References(s): PMID:25741868


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