Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2
  • Curation Notes: ClinVar Annotator: match by term: Seizures, scoliosis, and macrocephaly syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2


  • An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2
  • Curation Notes: ClinVar Annotator: match by term: Seizures, scoliosis, and macrocephaly syndrome
  • Original References(s): PMID:10713884 PMID:10750558 PMID:11432960 PMID:16283885 PMID:17041877 PMID:19344451 PMID:28492532 PMID:30288735 PMID:9326317


  • An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2
  • Curation Notes: ClinVar Annotator: match by term: Seizures, scoliosis, and macrocephaly syndrome


  • An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2
  • Curation Notes: ClinVar Annotator: match by term: Seizures, scoliosis, and macrocephaly syndrome
  • Original References(s): PMID:23439489 PMID:24728327 PMID:25741868 PMID:28492532


  • An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2
  • Curation Notes: ClinVar Annotator: match by term: Seizures, scoliosis, and macrocephaly syndrome
  • Original References(s): PMID:25741868 PMID:30997052


  • An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2
  • Curation Notes: ClinVar Annotator: match by term: Seizures, scoliosis, and macrocephaly syndrome
  • Original References(s): PMID:30288735


  • An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2
  • Curation Notes: ClinVar Annotator: match by term: Seizures, scoliosis, and macrocephaly syndrome
  • Original References(s): PMID:24728327 PMID:25741868 PMID:28492532 PMID:30997052


  • An association has been curated linking Ext2 and SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME 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 EXT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  (DOID:9009204)
  • 7 papers in RGD have been used to annotate Ext2
  • Curation Notes: ClinVar Annotator: match by term: Seizures, scoliosis, and macrocephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • Go Back to source page   Continue to Ontology report