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GENE - TERM ANNOTATION REPORT

26 Annotations Found.

An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by OMIM:253700


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by OMIM:253700
  • Original References(s): PMID:8923014


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by OMIM:253700
  • Original References(s): PMID:10874299 PMID:8923014


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:28492532


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Al-Zaidy SA, etal., Mol Genet Genomic Med. 2015 Mar;3(2):92-8. doi: 10.1002/mgg3.125. Epub 2015 Jan 8.
  • The annotation has been inferred from sequence orthology with SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 additional annotations were made from Al-Zaidy SA, etal., Mol Genet Genomic Med. 2015 Mar;3(2):92-8. doi: 10.1002/mgg3.125. Epub 2015 Jan 8.
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: DNA:mutation:cds: c.787G>A(p.Glu263Lys) (human)


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by OMIM:253700
  • Original References(s): PMID:10942431 PMID:1303286 PMID:7481775 PMID:8923014


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:10447257 PMID:15322984 PMID:18285821 PMID:22095924 PMID:28492532 PMID:8968757 PMID:9781048


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:25741868


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:18421900 PMID:28492532


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:18414213 PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:10942431 PMID:12040521 PMID:12566530 PMID:20623375 PMID:22240777 PMID:23929688 PMID:24033266 PMID:24552312 PMID:25741868 PMID:26467025 PMID:28492532 PMID:32214227 PMID:7481775 PMID:8923014


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:22095924


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2C
  • Original References(s): PMID:27708273


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:24033266


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:10447257 PMID:14981741 PMID:15322984 PMID:15479193 PMID:20345928 PMID:22095924 PMID:25741868 PMID:28492532 PMID:8968757 PMID:9658457 PMID:9781048


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:26467025


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:18285821 PMID:28492532


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:22095924 PMID:28492532 PMID:8968757 PMID:9781048


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:16832103 PMID:18285821 PMID:22095924 PMID:24534832 PMID:25802879 PMID:26467025 PMID:27708273 PMID:28492532


  • An association has been curated linking Sgcg and autosomal recessive limb-girdle muscular dystrophy type 2C 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 SGCG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2C  (DOID:0110277)
  • 12 papers in RGD have been used to annotate Sgcg
  • Curation Notes: ClinVar Annotator: match by term: Severe autosomal recessive muscular dystrophy of childhood - North African type
  • Original References(s): PMID:19770540 PMID:22095924 PMID:25605665 PMID:25741868 PMID:28492532 PMID:9673983


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