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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:12791812|RGD:401928384|RGD:405852256|RGD:408394191 (Homo sapiens) & RGD:12791812|RGD:401928384|RGD:405852256|RGD:408394191 (Homo sapiens) & RGD:12791812|RGD:401928384|RGD:405852256|RGD:408394191 (Homo sapiens) & RGD:12791812|RGD:401928384|RGD:405852256|RGD:408394191 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:25741868


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:8597928 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:19668217 PMID:9326342 PMID:9792859


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:151721653 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:28492532 PMID:34745210


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:155644592 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28513611 PMID:30457409 PMID:35882526


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:402517448 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:28492532 PMID:28513611


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:13618690 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:11170889 PMID:11589884 PMID:14506133 PMID:16936096 PMID:27124303 PMID:28492532


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:402515520 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:20881294 PMID:28492532


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens) & RGD:10049406|RGD:15177200|RGD:151889449|RGD:152124307|RGD:155993986|RGD:156049241|RGD:156276480|RGD:156352396|RGD:156406094|RGD:156449947|RGD:26892406|RGD:402518207|RGD:405155162|RGD:405163940|RGD:405247907 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:28492532


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:127248081|RGD:26890703 (Homo sapiens) & RGD:127248081|RGD:26890703 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:11170889 PMID:16936096 PMID:20881294 PMID:28492532


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:12791786 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:25786029 PMID:28492532 PMID:28513611


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:11560070|RGD:155644604|RGD:155644605|RGD:155644606|RGD:9692940 (Homo sapiens) & RGD:11560070|RGD:155644604|RGD:155644605|RGD:155644606|RGD:9692940 (Homo sapiens) & RGD:11560070|RGD:155644604|RGD:155644605|RGD:155644606|RGD:9692940 (Homo sapiens) & RGD:11560070|RGD:155644604|RGD:155644605|RGD:155644606|RGD:9692940 (Homo sapiens) & RGD:11560070|RGD:155644604|RGD:155644605|RGD:155644606|RGD:9692940 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:25741868 PMID:35882526


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:11560054|RGD:151840857 (Homo sapiens) & RGD:11560054|RGD:151840857 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:14506133 PMID:14578375 PMID:17197537 PMID:28492532 PMID:28513611 PMID:32631953


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:12791309|RGD:12791801|RGD:150436159 (Homo sapiens) & RGD:12791309|RGD:12791801|RGD:150436159 (Homo sapiens) & RGD:12791309|RGD:12791801|RGD:150436159 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3


    • An association has been curated linking LOC129995601 and Axenfeld-Rieger syndrome type 3 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:13490602|RGD:13810658 (Homo sapiens) & RGD:13490602|RGD:13810658 (Homo sapiens)
  • 25 RGD objects have been annotated to Axenfeld-Rieger syndrome type 3  (DOID:0110122)
  • 0 papers in RGD have been used to annotate LOC129995601
  • Curation Notes: ClinVar Annotator: match by term: Axenfeld-Rieger syndrome type 3
  • Original References(s): PMID:20881294 PMID:22382802 PMID:28492532


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