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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking B9D2 and Meckel Syndrome 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8568680 (Homo sapiens)
  • 2 RGD objects have been annotated to Meckel Syndrome 10  (DOID:9004364)
  • 4 papers in RGD have been used to annotate B9D2
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome, type 10
  • Original References(s): PMID:21763481


    • An association has been curated linking B9D2 and Meckel Syndrome 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to Meckel Syndrome 10  (DOID:9004364)
  • 4 papers in RGD have been used to annotate B9D2


    • An association has been curated linking B9D2 and Meckel Syndrome 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11642195|RGD:150407345|RGD:150407347|RGD:150407349|RGD:21404727 (Homo sapiens) & RGD:11642195|RGD:150407345|RGD:150407347|RGD:150407349|RGD:21404727 (Homo sapiens) & RGD:11642195|RGD:150407345|RGD:150407347|RGD:150407349|RGD:21404727 (Homo sapiens) & RGD:11642195|RGD:150407345|RGD:150407347|RGD:150407349|RGD:21404727 (Homo sapiens) & RGD:11642195|RGD:150407345|RGD:150407347|RGD:150407349|RGD:21404727 (Homo sapiens)
  • 2 RGD objects have been annotated to Meckel Syndrome 10  (DOID:9004364)
  • 4 papers in RGD have been used to annotate B9D2
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome, type 10
  • Original References(s): PMID:25741868


    • An association has been curated linking B9D2 and Meckel Syndrome 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:21071063 (Homo sapiens)
  • 2 RGD objects have been annotated to Meckel Syndrome 10  (DOID:9004364)
  • 4 papers in RGD have been used to annotate B9D2
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome, type 10
  • Original References(s): PMID:25741868 PMID:31411728


    • An association has been curated linking B9D2 and Meckel Syndrome 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10448345 (Homo sapiens)
  • 2 RGD objects have been annotated to Meckel Syndrome 10  (DOID:9004364)
  • 4 papers in RGD have been used to annotate B9D2
  • Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 34
  • Original References(s): PMID:26092869


    • An association has been curated linking B9D2 and Meckel Syndrome 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11654048 (Homo sapiens)
  • 2 RGD objects have been annotated to Meckel Syndrome 10  (DOID:9004364)
  • 4 papers in RGD have been used to annotate B9D2
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome, type 10
  • Original References(s): PMID:28492532


    • An association has been curated linking B9D2 and Meckel Syndrome 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10448358|RGD:10448373 (Homo sapiens) & RGD:10448358|RGD:10448373 (Homo sapiens)
  • 2 RGD objects have been annotated to Meckel Syndrome 10  (DOID:9004364)
  • 4 papers in RGD have been used to annotate B9D2
  • Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 34
  • Original References(s): PMID:26092869 PMID:28771248 PMID:33234550


    • An association has been curated linking B9D2 and Meckel Syndrome 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11546524|RGD:11549616|RGD:11550038 (Homo sapiens) & RGD:11546524|RGD:11549616|RGD:11550038 (Homo sapiens) & RGD:11546524|RGD:11549616|RGD:11550038 (Homo sapiens)
  • 2 RGD objects have been annotated to Meckel Syndrome 10  (DOID:9004364)
  • 4 papers in RGD have been used to annotate B9D2
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome, type 10
  • Original References(s): PMID:25741868 PMID:28492532


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