Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by OMIM:601954


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by OMIM:601954
  • Original References(s): PMID:25326637


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by OMIM:601954
  • Original References(s): PMID:10655062


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:25741868


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:15582318 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:16911908 PMID:18585512 PMID:19412328 PMID:20215591 PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:19035361 PMID:20474083 PMID:22194935 PMID:23299917 PMID:23861362 PMID:24033266 PMID:24037902 PMID:25741868 PMID:26350513 PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy type 2G
  • Original References(s): PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:18414213 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy type 2G
  • Original References(s): PMID:24037902 PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:24033266 PMID:24503780 PMID:25741868 PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy type 2G
  • Original References(s): PMID:24033266 PMID:24503780 PMID:25741868 PMID:26467025 PMID:27532257 PMID:28492532


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:23861362 PMID:24033266 PMID:24037902 PMID:25741868 PMID:26332198 PMID:26467025 PMID:28492532 PMID:30871747


  • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in CRRD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • Go Back to source page   Continue to Ontology report