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GENE - TERM ANNOTATION REPORT

17 Annotations Found.

An association has been curated linking SAMD9 and MIRAGE 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:40813822 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30046003


    • An association has been curated linking SAMD9 and MIRAGE 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:151730845 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MYELODYSPLASIA, INFECTION, RESTRICTION OF GROWTH, ADRENAL HYPOPLASIA, GENITAL PHENOTYPES, AND ENTEROPATHY
  • Original References(s): PMID:25741868 PMID:27182967 PMID:28492532 PMID:29266745 PMID:31620126


    • An association has been curated linking SAMD9 and MIRAGE 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:41406988 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MYELODYSPLASIA, INFECTION, RESTRICTION OF GROWTH, ADRENAL HYPOPLASIA, GENITAL PHENOTYPES, AND ENTEROPATHY
  • Original References(s): PMID:25741868 PMID:28346228 PMID:29266745 PMID:32106287 PMID:33237688


    • An association has been curated linking SAMD9 and MIRAGE 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:11531255 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:27182967 PMID:28346228 PMID:28492532 PMID:31666768 PMID:33237688


    • An association has been curated linking SAMD9 and MIRAGE 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:13532655 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:16960814 PMID:18094730 PMID:24029230 PMID:27182967 PMID:29365320 PMID:31208161 PMID:31638924 PMID:33237688


    • An association has been curated linking SAMD9 and MIRAGE 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:11531229 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:27182967


    • An association has been curated linking SAMD9 and MIRAGE Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9


    • An association has been curated linking SAMD9 and MIRAGE 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:155796787 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:25741868 PMID:33237688 PMID:34621053


    • An association has been curated linking SAMD9 and MIRAGE Syndrome in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking SAMD9 and MIRAGE 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:40886857 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MYELODYSPLASIA, INFECTION, RESTRICTION OF GROWTH, ADRENAL HYPOPLASIA, GENITAL PHENOTYPES, AND ENTEROPATHY
  • Original References(s): PMID:25741868 PMID:28346228 PMID:28492532 PMID:29506479 PMID:31231135 PMID:33237688


    • An association has been curated linking SAMD9 and MIRAGE 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:13784052 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:25741868 PMID:28346228 PMID:28492532 PMID:31231135


    • An association has been curated linking SAMD9 and MIRAGE 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:12893448 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:25741868 PMID:28346228 PMID:31309983


    • An association has been curated linking SAMD9 and MIRAGE 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:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens) & RGD:126746784|RGD:126774858|RGD:13790636|RGD:13827662|RGD:150333172|RGD:15097625|RGD:151355167|RGD:151356366|RGD:15166206|RGD:15192113|RGD:155800580 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome | ClinVar Annotator: match by term: MYELODYSPLASIA, INFECTION, RESTRICTION OF GROWTH, ADRENAL HYPOPLASIA, GENITAL PHENOTYPES, AND ENTEROPATHY
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SAMD9 and MIRAGE 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:11531247|RGD:153000634 (Homo sapiens) & RGD:11531247|RGD:153000634 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:25741868 PMID:27182967


    • An association has been curated linking SAMD9 and MIRAGE 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:126757213|RGD:150557185|RGD:151742690|RGD:155646004|RGD:156332203 (Homo sapiens) & RGD:126757213|RGD:150557185|RGD:151742690|RGD:155646004|RGD:156332203 (Homo sapiens) & RGD:126757213|RGD:150557185|RGD:151742690|RGD:155646004|RGD:156332203 (Homo sapiens) & RGD:126757213|RGD:150557185|RGD:151742690|RGD:155646004|RGD:156332203 (Homo sapiens) & RGD:126757213|RGD:150557185|RGD:151742690|RGD:155646004|RGD:156332203 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome
  • Original References(s): PMID:28492532


    • An association has been curated linking SAMD9 and MIRAGE 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:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens) & RGD:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens) & RGD:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens) & RGD:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens) & RGD:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens) & RGD:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens) & RGD:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens) & RGD:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens) & RGD:126746777|RGD:126746780|RGD:14695785|RGD:151350071|RGD:152061851|RGD:155800685|RGD:243050511|RGD:401918251|RGD:401940498 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome | ClinVar Annotator: match by term: MYELODYSPLASIA, INFECTION, RESTRICTION OF GROWTH, ADRENAL HYPOPLASIA, GENITAL PHENOTYPES, AND ENTEROPATHY
  • Original References(s): PMID:25741868


    • An association has been curated linking SAMD9 and MIRAGE 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:150557181|RGD:151663744|RGD:15173950|RGD:152978546|RGD:153301121 (Homo sapiens) & RGD:150557181|RGD:151663744|RGD:15173950|RGD:152978546|RGD:153301121 (Homo sapiens) & RGD:150557181|RGD:151663744|RGD:15173950|RGD:152978546|RGD:153301121 (Homo sapiens) & RGD:150557181|RGD:151663744|RGD:15173950|RGD:152978546|RGD:153301121 (Homo sapiens) & RGD:150557181|RGD:151663744|RGD:15173950|RGD:152978546|RGD:153301121 (Homo sapiens)
  • 1 RGD objects have been annotated to MIRAGE Syndrome  (DOID:9009218)
  • 4 papers in RGD have been used to annotate SAMD9
  • Curation Notes: ClinVar Annotator: match by term: MIRAGE syndrome


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