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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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:11531336 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, davignon-chauveau type
  • Original References(s): PMID:27008887


    • An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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 Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4


    • An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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:38597463 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, davignon-chauveau type
  • Original References(s): PMID:25741868 PMID:31794073


    • An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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:150545884 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4
  • Curation Notes: ClinVar Annotator: match by term: TRIP4-Related Disorders


    • An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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:401867593 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4
  • Curation Notes: ClinVar Annotator: match by term: TRIP4-Related Disorders
  • Original References(s): PMID:16199547 PMID:26924529 PMID:27008887 PMID:28492532 PMID:35372177


    • An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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:150545883|RGD:15119228|RGD:15135397|RGD:15138629|RGD:15167902 (Homo sapiens) & RGD:150545883|RGD:15119228|RGD:15135397|RGD:15138629|RGD:15167902 (Homo sapiens) & RGD:150545883|RGD:15119228|RGD:15135397|RGD:15138629|RGD:15167902 (Homo sapiens) & RGD:150545883|RGD:15119228|RGD:15135397|RGD:15138629|RGD:15167902 (Homo sapiens) & RGD:150545883|RGD:15119228|RGD:15135397|RGD:15138629|RGD:15167902 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4
  • Curation Notes: ClinVar Annotator: match by term: TRIP4-Related Disorders
  • Original References(s): PMID:28492532


    • An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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:126726681|RGD:150464857|RGD:15157838|RGD:15200342|RGD:156128739 (Homo sapiens) & RGD:126726681|RGD:150464857|RGD:15157838|RGD:15200342|RGD:156128739 (Homo sapiens) & RGD:126726681|RGD:150464857|RGD:15157838|RGD:15200342|RGD:156128739 (Homo sapiens) & RGD:126726681|RGD:150464857|RGD:15157838|RGD:15200342|RGD:156128739 (Homo sapiens) & RGD:126726681|RGD:150464857|RGD:15157838|RGD:15200342|RGD:156128739 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, davignon-chauveau type | ClinVar Annotator: match by term: TRIP4-Related Disorders
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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:150476102|RGD:151235270 (Homo sapiens) & RGD:150476102|RGD:151235270 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, congenital, davignon-chauveau type
  • Original References(s): PMID:25741868


    • An association has been curated linking TRIP4 and Congenital Muscular Dystrophy, Davignon-Chauveau Type 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:150545236 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Muscular Dystrophy, Davignon-Chauveau Type  (DOID:9006286)
  • 3 papers in RGD have been used to annotate TRIP4
  • Curation Notes: ClinVar Annotator: match by term: TRIP4-Related Disorders
  • Original References(s): PMID:25741868 PMID:26924529 PMID:27008887 PMID:28492532


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