Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes QTLs Strains Markers Genome Information Ontologies Cell Lines References FTP Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) RatMine GViewer (Genome Viewer) Overgo Probe Designer ACP Haplotyper Genome Scanner
Aging & Age-Related Disease Cancer Cardiovascular Disease COVID-19 Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models PhenoMiner (Quantitative Phenotypes) Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes GERRC (Gene Editing Rat Resource Center) 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 Poster Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

GENE - TERM ANNOTATION REPORT

27 Annotations Found.

An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by OMIM:603358
  • Original References(s): PMID:12215968


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by OMIM:603358
  • Original References(s): PMID:19285991


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:12910490 PMID:20727375 PMID:28322498 PMID:28492532


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by OMIM:603358


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:11528392 PMID:12215968 PMID:12547234 PMID:18386115 PMID:19508421 PMID:21274865 PMID:25741868 PMID:25914718 PMID:28492532


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:11528392 PMID:17314340 PMID:20518024 PMID:23892085 PMID:24655110 PMID:28492532 PMID:29090881


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:25895478 PMID:28492532


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24033266


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:28492532


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:28105683


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17403714 PMID:24033266


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:26489029


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17314340 PMID:17403714 PMID:27959697 PMID:28492532 PMID:30582773 PMID:31435670


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:28322498


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24236502 PMID:26489029


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:12215968 PMID:22277166


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:19389488 PMID:28496993


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24033266 PMID:26467025


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17314340 PMID:17403714 PMID:20518024


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17403714 PMID:22310368


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:18771761 PMID:24033266 PMID:26467025


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:12215968 PMID:17314340 PMID:25895478 PMID:28492532


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:12215968 PMID:12910490 PMID:19389488 PMID:19508421 PMID:20518024 PMID:22277166 PMID:25741868 PMID:28492532


    • An association has been curated linking Bcs1l and GRACILE syndrome 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 BCS1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to GRACILE syndrome  (DOID:0111455)
  • 10 papers in RGD have been used to annotate Bcs1l
  • Curation Notes: ClinVar Annotator: match by term: GRACILE syndrome
  • Original References(s): PMID:17314340 PMID:25741868 PMID:28492532


    • Go Back to source page   Continue to Ontology report