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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by OMIM:177170
  • Original References(s): PMID:7670471


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by term: Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Original References(s): PMID:11782471 PMID:11968079 PMID:7670471 PMID:9463320 PMID:9887340


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by term: Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Original References(s): PMID:9632164 PMID:9921895


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by OMIM:177170


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by OMIM:177170
  • Original References(s): PMID:11746045


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by OMIM:177170
  • Original References(s): PMID:11746044


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by OMIM:177170
  • Original References(s): PMID:7670472


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by OMIM:177170
  • Original References(s): PMID:12483304


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by OMIM:177170
  • Original References(s): PMID:11968079 PMID:7670472 PMID:9463320


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by term: Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:7670471 PMID:7670472 PMID:9887340


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by term: Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by term: Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by term: Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Original References(s): PMID:24595329


  • An association has been curated linking Comp and pseudoachondroplasia 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 COMP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudoachondroplasia  (DOID:0080047)
  • 17 papers in RGD have been used to annotate Comp
  • Curation Notes: ClinVar Annotator: match by term: Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Original References(s): PMID:12768438 PMID:25741868


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