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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by term: Chondrodysplasia punctata 2, X-linked dominant, atypical
  • Original References(s): PMID:22229330


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:10391219


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:10942423


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:18414213


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:10391219 PMID:12503102 PMID:18414213


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:10942423 PMID:12483303 PMID:1355069 PMID:18414213 PMID:7677157


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:25741868


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:10391218 PMID:10391219


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:10391218


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by OMIM:302960
  • Original References(s): PMID:18414213 PMID:20949533


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by term: Chondrodysplasia punctata 2 X-linked dominant
  • Original References(s): PMID:15368506


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by term: Chondrodysplasia punctata 2 X-linked dominant
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by term: Chondrodysplasia punctata 2 X-linked dominant
  • Original References(s): PMID:18414213 PMID:28492532


    • An association has been curated linking Ebp and X-linked chondrodysplasia punctata 2 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 EBP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked chondrodysplasia punctata 2  (DOID:0080352)
  • 13 papers in RGD have been used to annotate Ebp
  • Curation Notes: ClinVar Annotator: match by term: Chondrodysplasia punctata 2 X-linked dominant


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