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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking TSPEAR 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:11091550 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266


    • An association has been curated linking TSPEAR 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:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens) & RGD:150431518|RGD:150553222|RGD:151351571|RGD:155928747|RGD:155946521|RGD:155968873|RGD:155985895|RGD:156019470|RGD:156062431|RGD:156064202|RGD:156115530|RGD:156191881|RGD:156233410|RGD:156286642|RGD:156306340|RGD:156308538|RGD:156347641|RGD:156401864|RGD:329377688|RGD:401757668|RGD:401760966|RGD:401882150|RGD:405798957|RGD:405798961|RGD:405798964|RGD:405798973|RGD:405798980 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking TSPEAR 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:13539221 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:22678063 PMID:24033266 PMID:25741868 PMID:27736875 PMID:28492532 PMID:30544257 PMID:32112661 PMID:34042254


    • An association has been curated linking TSPEAR 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:11088250|RGD:11088548|RGD:11091037|RGD:13535039 (Homo sapiens) & RGD:11088250|RGD:11088548|RGD:11091037|RGD:13535039 (Homo sapiens) & RGD:11088250|RGD:11088548|RGD:11091037|RGD:13535039 (Homo sapiens) & RGD:11088250|RGD:11088548|RGD:11091037|RGD:13535039 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking TSPEAR 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:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens) & RGD:13833413|RGD:150407437|RGD:150409547|RGD:150418911|RGD:150420596|RGD:150425181|RGD:150547957|RGD:151234675|RGD:151800000|RGD:151832795|RGD:151835505|RGD:155802781|RGD:155966188|RGD:156137776|RGD:156247094|RGD:156261570|RGD:156367209|RGD:401726237|RGD:401730117 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking TSPEAR 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:11092255 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266 PMID:25741868 PMID:25855803 PMID:26467025 PMID:27736875 PMID:28492532 PMID:29144512 PMID:30046887 PMID:34042254


    • An association has been curated linking TSPEAR 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:12896875 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266 PMID:25741868 PMID:27736875 PMID:28492532 PMID:34042254


    • An association has been curated linking TSPEAR 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:13536729|RGD:15101002|RGD:151823383|RGD:151860703 (Homo sapiens) & RGD:13536729|RGD:15101002|RGD:151823383|RGD:151860703 (Homo sapiens) & RGD:13536729|RGD:15101002|RGD:151823383|RGD:151860703 (Homo sapiens) & RGD:13536729|RGD:15101002|RGD:151823383|RGD:151860703 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking TSPEAR 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:11091962|RGD:13538689 (Homo sapiens) & RGD:11091962|RGD:13538689 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking TSPEAR 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:25317639 (Homo sapiens)
  • 23830 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate TSPEAR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:26969326 PMID:27736875 PMID:28492532 PMID:30046887 PMID:34042254


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