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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:11577744 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: ARTHROGRYPOSIS MULTIPLEX CONGENITA, MYOGENIC TYPE
  • Original References(s): PMID:25741868 PMID:26467025 PMID:27086870 PMID:27178001 PMID:28492532


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:8556750 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:19542096 PMID:27782104


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:11636632 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:24838835 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:11577841 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:25741868 PMID:26467025 PMID:26539891 PMID:28492532


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens) & RGD:11542861|RGD:11544149|RGD:11544207|RGD:11545541|RGD:11548437|RGD:11549159|RGD:11549426|RGD:11550003|RGD:11551305|RGD:11552156|RGD:11584716|RGD:126725674|RGD:126725684|RGD:127286074|RGD:14715259|RGD:151348035|RGD:155265527|RGD:155265528|RGD:155644567|RGD:401854899|RGD:401854901|RGD:401855041|RGD:401856646|RGD:40815242|RGD:40815244 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:25741868


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:14698082 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:25741868 PMID:27782104


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:11543936 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:25741868 PMID:26467025


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens) & RGD:10049035|RGD:10049046|RGD:10049782|RGD:11577433|RGD:11586137|RGD:11639717|RGD:21068173|RGD:8660756|RGD:8660760|RGD:8660761|RGD:8660765|RGD:8660767|RGD:8660772|RGD:8660776|RGD:8660780|RGD:8660787|RGD:8660798|RGD:8660806|RGD:8660808|RGD:8660819 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: ARTHROGRYPOSIS MULTIPLEX CONGENITA, MYOGENIC TYPE | ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:11658797 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:24319099 PMID:25741868 PMID:26467025


    • An association has been curated linking SYNE1 and arthrogryposis multiplex congenita-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:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens) & RGD:11544980|RGD:11548763|RGD:11550739|RGD:11551227|RGD:11551540|RGD:11552088|RGD:11635112|RGD:11638816|RGD:11643278|RGD:14706178|RGD:151831953 (Homo sapiens)
  • 4 RGD objects have been annotated to arthrogryposis multiplex congenita-3  (DOID:0080979)
  • 12 papers in RGD have been used to annotate SYNE1
  • Curation Notes: ClinVar Annotator: match by term: Arthrogryposis multiplex congenita 3, myogenic type
  • Original References(s): PMID:25741868 PMID:28492532


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