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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Tmco1 and Cerebrofaciothoracic Dysplasia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with TMCO1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Cerebrofaciothoracic Dysplasia  (DOID:9006917)
  • 7 papers in RGD have been used to annotate Tmco1
  • Curation Notes: ClinVar Annotator: match by term: Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
  • Original References(s): PMID:20018682, PMID:23320496, PMID:24033266, PMID:24194475, PMID:24424126


  • An association has been curated linking Tmco1 and Cerebrofaciothoracic Dysplasia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with TMCO1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Cerebrofaciothoracic Dysplasia  (DOID:9006917)
  • 7 papers in RGD have been used to annotate Tmco1
  • Curation Notes: ClinVar Annotator: match by synonym: Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
  • Original References(s): PMID:17351359, PMID:23320496, PMID:24194475


  • An association has been curated linking Tmco1 and Cerebrofaciothoracic Dysplasia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with TMCO1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Cerebrofaciothoracic Dysplasia  (DOID:9006917)
  • 7 papers in RGD have been used to annotate Tmco1


  • An association has been curated linking Tmco1 and Cerebrofaciothoracic Dysplasia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with TMCO1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Cerebrofaciothoracic Dysplasia  (DOID:9006917)
  • 7 papers in RGD have been used to annotate Tmco1
  • Curation Notes: ClinVar Annotator: match by term: Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
  • Original References(s): PMID:25741868, PMID:31102500, PMID:32214227


  • An association has been curated linking Tmco1 and Cerebrofaciothoracic Dysplasia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with TMCO1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Cerebrofaciothoracic Dysplasia  (DOID:9006917)
  • 7 papers in RGD have been used to annotate Tmco1
  • Curation Notes: ClinVar Annotator: match by term: Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Tmco1 and Cerebrofaciothoracic Dysplasia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with TMCO1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Cerebrofaciothoracic Dysplasia  (DOID:9006917)
  • 7 papers in RGD have been used to annotate Tmco1
  • Curation Notes: ClinVar Annotator: match by term: Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
  • Original References(s): PMID:23806086, PMID:24088041, PMID:24424126


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.