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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking TMTC3 and lissencephaly 8 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 lissencephaly 8  (DOID:0112233)
  • 2 papers in RGD have been used to annotate TMTC3


    • An association has been curated linking TMTC3 and lissencephaly 8 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:12738847 (Homo sapiens)
  • 1 RGD objects have been annotated to lissencephaly 8  (DOID:0112233)
  • 2 papers in RGD have been used to annotate TMTC3
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 8
  • Original References(s): PMID:25741868 PMID:27773428 PMID:28097321


    • An association has been curated linking TMTC3 and lissencephaly 8 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:12738806|RGD:12740621|RGD:12740628|RGD:12740637 (Homo sapiens) & RGD:12738806|RGD:12740621|RGD:12740628|RGD:12740637 (Homo sapiens) & RGD:12738806|RGD:12740621|RGD:12740628|RGD:12740637 (Homo sapiens) & RGD:12738806|RGD:12740621|RGD:12740628|RGD:12740637 (Homo sapiens)
  • 1 RGD objects have been annotated to lissencephaly 8  (DOID:0112233)
  • 2 papers in RGD have been used to annotate TMTC3
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 8
  • Original References(s): PMID:27773428


    • An association has been curated linking TMTC3 and lissencephaly 8 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:126738740|RGD:243063005|RGD:404999698|RGD:405700498|RGD:407474938|RGD:596922032 (Homo sapiens) & RGD:126738740|RGD:243063005|RGD:404999698|RGD:405700498|RGD:407474938|RGD:596922032 (Homo sapiens) & RGD:126738740|RGD:243063005|RGD:404999698|RGD:405700498|RGD:407474938|RGD:596922032 (Homo sapiens) & RGD:126738740|RGD:243063005|RGD:404999698|RGD:405700498|RGD:407474938|RGD:596922032 (Homo sapiens) & RGD:126738740|RGD:243063005|RGD:404999698|RGD:405700498|RGD:407474938|RGD:596922032 (Homo sapiens) & RGD:126738740|RGD:243063005|RGD:404999698|RGD:405700498|RGD:407474938|RGD:596922032 (Homo sapiens)
  • 1 RGD objects have been annotated to lissencephaly 8  (DOID:0112233)
  • 2 papers in RGD have been used to annotate TMTC3
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 8
  • Original References(s): PMID:25741868


    • An association has been curated linking TMTC3 and lissencephaly 8 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:151662716|RGD:151740119 (Homo sapiens) & RGD:151662716|RGD:151740119 (Homo sapiens)
  • 1 RGD objects have been annotated to lissencephaly 8  (DOID:0112233)
  • 2 papers in RGD have been used to annotate TMTC3
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 8
  • Original References(s): PMID:25741868 PMID:27773428 PMID:28492532 PMID:28973161


    • An association has been curated linking TMTC3 and lissencephaly 8 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:15129180|RGD:15154193|RGD:15163639|RGD:152065560|RGD:152076399|RGD:152124111|RGD:156382911|RGD:405279290 (Homo sapiens) & RGD:15129180|RGD:15154193|RGD:15163639|RGD:152065560|RGD:152076399|RGD:152124111|RGD:156382911|RGD:405279290 (Homo sapiens) & RGD:15129180|RGD:15154193|RGD:15163639|RGD:152065560|RGD:152076399|RGD:152124111|RGD:156382911|RGD:405279290 (Homo sapiens) & RGD:15129180|RGD:15154193|RGD:15163639|RGD:152065560|RGD:152076399|RGD:152124111|RGD:156382911|RGD:405279290 (Homo sapiens) & RGD:15129180|RGD:15154193|RGD:15163639|RGD:152065560|RGD:152076399|RGD:152124111|RGD:156382911|RGD:405279290 (Homo sapiens) & RGD:15129180|RGD:15154193|RGD:15163639|RGD:152065560|RGD:152076399|RGD:152124111|RGD:156382911|RGD:405279290 (Homo sapiens) & RGD:15129180|RGD:15154193|RGD:15163639|RGD:152065560|RGD:152076399|RGD:152124111|RGD:156382911|RGD:405279290 (Homo sapiens) & RGD:15129180|RGD:15154193|RGD:15163639|RGD:152065560|RGD:152076399|RGD:152124111|RGD:156382911|RGD:405279290 (Homo sapiens)
  • 1 RGD objects have been annotated to lissencephaly 8  (DOID:0112233)
  • 2 papers in RGD have been used to annotate TMTC3
  • Curation Notes: ClinVar Annotator: match by term: TMTC3-related condition
  • Original References(s): PMID:28492532


    • An association has been curated linking TMTC3 and lissencephaly 8 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:126738733|RGD:15107914|RGD:15165071|RGD:151783921|RGD:151829863|RGD:152035421|RGD:156000513 (Homo sapiens) & RGD:126738733|RGD:15107914|RGD:15165071|RGD:151783921|RGD:151829863|RGD:152035421|RGD:156000513 (Homo sapiens) & RGD:126738733|RGD:15107914|RGD:15165071|RGD:151783921|RGD:151829863|RGD:152035421|RGD:156000513 (Homo sapiens) & RGD:126738733|RGD:15107914|RGD:15165071|RGD:151783921|RGD:151829863|RGD:152035421|RGD:156000513 (Homo sapiens) & RGD:126738733|RGD:15107914|RGD:15165071|RGD:151783921|RGD:151829863|RGD:152035421|RGD:156000513 (Homo sapiens) & RGD:126738733|RGD:15107914|RGD:15165071|RGD:151783921|RGD:151829863|RGD:152035421|RGD:156000513 (Homo sapiens) & RGD:126738733|RGD:15107914|RGD:15165071|RGD:151783921|RGD:151829863|RGD:152035421|RGD:156000513 (Homo sapiens)
  • 1 RGD objects have been annotated to lissencephaly 8  (DOID:0112233)
  • 2 papers in RGD have been used to annotate TMTC3
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 8 | ClinVar Annotator: match by term: TMTC3-related condition
  • Original References(s): PMID:25741868 PMID:28492532


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