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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:14396506 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome
  • Original References(s): PMID:28296084 PMID:31334757


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:151749106 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome
  • Original References(s): PMID:28492532


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:14396409 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome
  • Original References(s): PMID:29263825


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:14396412 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome
  • Original References(s): PMID:25741868 PMID:30765867


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:21074867 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome
  • Original References(s): PMID:28492532 PMID:33619735


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:14396410 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome
  • Original References(s): PMID:30447054


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:21074866|RGD:401857260|RGD:401963964|RGD:405291362 (Homo sapiens) & RGD:21074866|RGD:401857260|RGD:401963964|RGD:405291362 (Homo sapiens) & RGD:21074866|RGD:401857260|RGD:401963964|RGD:405291362 (Homo sapiens) & RGD:21074866|RGD:401857260|RGD:401963964|RGD:405291362 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:126728156|RGD:152067370|RGD:152085001 (Homo sapiens) & RGD:126728156|RGD:152067370|RGD:152085001 (Homo sapiens) & RGD:126728156|RGD:152067370|RGD:152085001 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens) & RGD:126728153|RGD:150452625|RGD:150507252|RGD:151348032|RGD:151661327|RGD:151661328|RGD:155796923|RGD:155797228|RGD:243050274|RGD:243051960|RGD:401875264|RGD:401905276 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking STAG2 and Mullegama-Klein-Martinez syndrome 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:13794821|RGD:13794848|RGD:13794850 (Homo sapiens) & RGD:13794821|RGD:13794848|RGD:13794850 (Homo sapiens) & RGD:13794821|RGD:13794848|RGD:13794850 (Homo sapiens)
  • 2 RGD objects have been annotated to Mullegama-Klein-Martinez syndrome  (DOID:0111845)
  • 4 papers in RGD have been used to annotate STAG2
  • Curation Notes: ClinVar Annotator: match by term: STAG2-related disorder
  • Original References(s): PMID:25741868 PMID:30158690


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