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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking SFTA3 and choreatic disease 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:40887978 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:24555207


    • An association has been curated linking SFTA3 and choreatic disease 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:11621795 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SFTA3 and choreatic disease 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:14698839 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:23430038 PMID:24714694 PMID:25741868


    • An association has been curated linking SFTA3 and choreatic disease 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:8598127 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:16220345 PMID:28492532 PMID:28503612


    • An association has been curated linking SFTA3 and choreatic disease 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:40887142 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:24930029


    • An association has been curated linking SFTA3 and choreatic disease 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:14978402 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:25741868 PMID:30352709


    • An association has been curated linking SFTA3 and choreatic disease 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:8598123 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:11971878 PMID:25741868 PMID:28492532


    • An association has been curated linking SFTA3 and choreatic disease 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:8598126 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:15955952 PMID:23379327 PMID:24714694 PMID:25741868 PMID:28492532 PMID:29882472


    • An association has been curated linking SFTA3 and choreatic disease 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:13506340 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:19176457 PMID:28492532


    • An association has been curated linking SFTA3 and choreatic disease 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:8560814 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:12891678 PMID:15289765 PMID:17576681 PMID:24930029 PMID:28492532 PMID:9536098


    • An association has been curated linking SFTA3 and choreatic disease 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:13531890 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:25741868 PMID:26723978


    • An association has been curated linking SFTA3 and choreatic disease 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:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens) & RGD:11600554|RGD:11604106|RGD:11606611|RGD:11613885|RGD:11614302|RGD:11614879|RGD:11615537|RGD:11618174|RGD:11619180|RGD:11620528|RGD:11634605|RGD:11634648|RGD:11635142|RGD:11635221|RGD:11646240|RGD:11648611|RGD:11651660|RGD:11651866|RGD:11653761|RGD:11654053|RGD:152982467|RGD:152983163|RGD:21074817|RGD:28869836|RGD:28869839|RGD:28872443|RGD:28872446|RGD:28872685|RGD:28911855 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea


    • An association has been curated linking SFTA3 and choreatic disease 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:151856820 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:16220345 PMID:24129101 PMID:24714694 PMID:25741868 PMID:28492532


    • An association has been curated linking SFTA3 and choreatic disease 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:11612513|RGD:13517284|RGD:150520442|RGD:243052957|RGD:329952657|RGD:401860577 (Homo sapiens) & RGD:11612513|RGD:13517284|RGD:150520442|RGD:243052957|RGD:329952657|RGD:401860577 (Homo sapiens) & RGD:11612513|RGD:13517284|RGD:150520442|RGD:243052957|RGD:329952657|RGD:401860577 (Homo sapiens) & RGD:11612513|RGD:13517284|RGD:150520442|RGD:243052957|RGD:329952657|RGD:401860577 (Homo sapiens) & RGD:11612513|RGD:13517284|RGD:150520442|RGD:243052957|RGD:329952657|RGD:401860577 (Homo sapiens) & RGD:11612513|RGD:13517284|RGD:150520442|RGD:243052957|RGD:329952657|RGD:401860577 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea | ClinVar Annotator: match by term: HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA
  • Original References(s): PMID:25741868


    • An association has been curated linking SFTA3 and choreatic disease 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:11645533|RGD:11648612|RGD:15119070 (Homo sapiens) & RGD:11645533|RGD:11648612|RGD:15119070 (Homo sapiens) & RGD:11645533|RGD:11648612|RGD:15119070 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:28492532


    • An association has been curated linking SFTA3 and choreatic disease 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:8560812|RGD:8598122|RGD:8598124 (Homo sapiens) & RGD:8560812|RGD:8598122|RGD:8598124 (Homo sapiens) & RGD:8560812|RGD:8598122|RGD:8598124 (Homo sapiens)
  • 493 RGD objects have been annotated to choreatic disease  (DOID:12859)
  • 2 papers in RGD have been used to annotate SFTA3
  • Curation Notes: ClinVar Annotator: match by term: Benign hereditary chorea
  • Original References(s): PMID:11971878


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