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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking SERAC1 and genetic 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:13832969 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate SERAC1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33431980


    • An association has been curated linking SERAC1 and genetic 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:10411348|RGD:10411693 (Homo sapiens) & RGD:10411348|RGD:10411693 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate SERAC1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SERAC1 and genetic 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:26922826 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate SERAC1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


    • An association has been curated linking SERAC1 and genetic 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:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens) & RGD:156003132|RGD:156035706|RGD:156105286|RGD:156182480|RGD:156187372|RGD:156215382|RGD:156238227|RGD:156252890|RGD:156260203|RGD:329391204|RGD:401771504|RGD:401775661|RGD:405746310|RGD:405746320|RGD:405746330|RGD:405746338|RGD:407492418 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate SERAC1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking SERAC1 and genetic 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:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens) & RGD:10409866|RGD:126923781|RGD:12838483|RGD:13820407|RGD:151735776|RGD:151818965|RGD:151875080|RGD:156093908|RGD:156369976|RGD:156372793|RGD:26902299|RGD:38466613 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate SERAC1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


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