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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Ddhd1 and hereditary spastic paraplegia 28 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 DDHD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hereditary spastic paraplegia 28  (DOID:0110779)
  • 5 papers in RGD have been used to annotate Ddhd1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 28
  • Original References(s): PMID:15786464 PMID:17576681 PMID:23176821 PMID:24989667 PMID:25741868 PMID:26944165 PMID:27216551 PMID:27999540 PMID:28492532 PMID:28818478 PMID:9536098


    • An association has been curated linking Ddhd1 and hereditary spastic paraplegia 28 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 DDHD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hereditary spastic paraplegia 28  (DOID:0110779)
  • 5 papers in RGD have been used to annotate Ddhd1


    • An association has been curated linking Ddhd1 and hereditary spastic paraplegia 28 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with DDHD1 (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to hereditary spastic paraplegia 28  (DOID:0110779)
  • 5 papers in RGD have been used to annotate Ddhd1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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