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GENE - TERM ANNOTATION REPORT

17 Annotations Found.

An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Original References(s): PMID:25741868, PMID:27753269


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:112567, PMID:18513679


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:20830804


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:18513679


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:15368507, PMID:18513679, PMID:20830804


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:18513679, PMID:20830804


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:15098240, PMID:15215498


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:19320654


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:18698629


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:18513679, PMID:20830804, PMID:9039660


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by OMIM:143095
  • Original References(s): PMID:23918704


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia with congenital joint dislocations


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Original References(s): PMID:26402641, PMID:28492532, PMID:29453417


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Original References(s): PMID:28492532


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Original References(s): PMID:25741868


  • An association has been curated linking Chst3 and spondyloepiphyseal dysplasia with congenital joint dislocations 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 CHST3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to spondyloepiphyseal dysplasia with congenital joint dislocations  (DOID:0050813)
  • 12 papers in CRRD have been used to annotate Chst3
  • Curation Notes: ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Original References(s): PMID:20830804, PMID:28492532, PMID:9039660


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.