Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Sgca and autosomal recessive limb-girdle muscular dystrophy 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 SGCA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 144 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 15 papers in RGD have been used to annotate Sgca
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy
  • Original References(s): PMID:10942431 PMID:12075495 PMID:12566530 PMID:12746421 PMID:15298081 PMID:17994539 PMID:18285821 PMID:18421900 PMID:18535179 PMID:18996010 PMID:19798725 PMID:21031578 PMID:22095924 PMID:24033266 PMID:24565866 PMID:24742800 PMID:25135358 PMID:25214167 PMID:25741868 PMID:26404900 PMID:26453141 PMID:26467025 PMID:26916285 PMID:26934379 PMID:27120200 PMID:28403181 PMID:28492532 PMID:29382405 PMID:30703231 PMID:30764848 PMID:30919934 PMID:31069529 PMID:31407473 PMID:31517061 PMID:31791368 PMID:31847883 PMID:35948506 PMID:7663524 PMID:7668821 PMID:8069911 PMID:9032047 PMID:9153448 PMID:9192266 PMID:9393893 PMID:9585331


    • An association has been curated linking Sgca and autosomal recessive limb-girdle muscular dystrophy 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 SGCA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 144 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 15 papers in RGD have been used to annotate Sgca
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy
  • Original References(s): PMID:10942431 PMID:10993494 PMID:12075495 PMID:12566530 PMID:12746421 PMID:15298081 PMID:15833425 PMID:17994539 PMID:18285821 PMID:18421900 PMID:18535179 PMID:18996010 PMID:19798725 PMID:21031578 PMID:22095924 PMID:24033266 PMID:24464767 PMID:24565866 PMID:24742800 PMID:25135358 PMID:25214167 PMID:25741868 PMID:25898921 PMID:26404900 PMID:26453141 PMID:26467025 PMID:26916285 PMID:26934379 PMID:27120200 PMID:28403181 PMID:28492532 PMID:29382405 PMID:30345904 PMID:30703231 PMID:30764848 PMID:30919934 PMID:31069529 PMID:31407473 PMID:31517061 PMID:31791368 PMID:31847883 PMID:35948506 PMID:7663524 PMID:7668821 PMID:8069911 PMID:9032047 PMID:9153448 PMID:9192266 PMID:9393893 PMID:9455986 PMID:9585331


    • An association has been curated linking Sgca and autosomal recessive limb-girdle muscular dystrophy 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 SGCA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 144 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 15 papers in RGD have been used to annotate Sgca
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy
  • Original References(s): PMID:10385046 PMID:10942431 PMID:10993494 PMID:11693784 PMID:12075495 PMID:12566530 PMID:12746421 PMID:15298081 PMID:15736300 PMID:15833425 PMID:16616845 PMID:16633953 PMID:16787395 PMID:17576681 PMID:17994539 PMID:18252745 PMID:18285821 PMID:18421900 PMID:18535179 PMID:18996010 PMID:19798725 PMID:21031578 PMID:21856579 PMID:22095924 PMID:24033266 PMID:24464767 PMID:24565866 PMID:24742800 PMID:25135358 PMID:25214167 PMID:25741868 PMID:25898921 PMID:26404900 PMID:26453141 PMID:26467025 PMID:26916285 PMID:26934379 PMID:27120200 PMID:28403181 PMID:28492532 PMID:29351619 PMID:29382405 PMID:30107846 PMID:30345904 PMID:30703231 PMID:30764848 PMID:30919934 PMID:31069529 PMID:31407473 PMID:31517061 PMID:31791368 PMID:31847883 PMID:32382396 PMID:33848270 PMID:34602496 PMID:35948506 PMID:7657792 PMID:7663524 PMID:7668821 PMID:8069911 PMID:8528203 PMID:8866424 PMID:9032047 PMID:9153448 PMID:9192266 PMID:9393893 PMID:9455986 PMID:9536098 PMID:9585331


    • An association has been curated linking Sgca and autosomal recessive limb-girdle muscular dystrophy 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 SGCA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 144 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 15 papers in RGD have been used to annotate Sgca
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy | ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, recessive
  • Original References(s): PMID:10385046 PMID:10942431 PMID:10993494 PMID:11693784 PMID:12075495 PMID:12566530 PMID:12746421 PMID:15298081 PMID:15736300 PMID:15833425 PMID:16199547 PMID:16616845 PMID:16633953 PMID:16787395 PMID:17576681 PMID:17994539 PMID:18252745 PMID:18285821 PMID:18421900 PMID:18535179 PMID:18996010 PMID:19798725 PMID:20623375 PMID:21031578 PMID:21856579 PMID:22095924 PMID:22303798 PMID:24033266 PMID:24464767 PMID:24565866 PMID:24742800 PMID:25135358 PMID:25214167 PMID:25741868 PMID:25898921 PMID:26404900 PMID:26453141 PMID:26467025 PMID:26916285 PMID:26934379 PMID:26944168 PMID:27120200 PMID:27906075 PMID:28403181 PMID:28492532 PMID:28687063 PMID:29351619 PMID:29382405 PMID:30107846 PMID:30345904 PMID:30703231 PMID:30764848 PMID:30838351 PMID:30919934 PMID:31061434 PMID:31069529 PMID:31127727 PMID:31130284 PMID:31268554 PMID:31407473 PMID:31517061 PMID:31791368 PMID:31847883 PMID:32382396 PMID:32528171 PMID:32875335 PMID:33386810 PMID:33726816 PMID:33848270 PMID:34602496 PMID:35416532 PMID:35948506 PMID:37273706 PMID:7657792 PMID:7663524 PMID:7668821 PMID:8069911 PMID:8528203 PMID:8866424 PMID:9032047 PMID:9153448 PMID:9192266 PMID:9393893 PMID:9455986 PMID:9536098 PMID:9585331


    • Go Back to source page   Continue to Ontology report