Send us a Message



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

GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking MECP2 and Neurodevelopmental Disorders in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 13563 RGD objects have been annotated to Neurodevelopmental Disorders  (DOID:9004429)
  • 23 papers in RGD have been used to annotate MECP2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:28191889 PMID:29942082


  • An association has been curated linking MECP2 and Neurodevelopmental Disorders 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:8562753 (Homo sapiens)
  • 13563 RGD objects have been annotated to Neurodevelopmental Disorders  (DOID:9004429)
  • 23 papers in RGD have been used to annotate MECP2
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder
  • Original References(s): PMID:11007980 PMID:11071498 PMID:11309367 PMID:11772708 PMID:11805248 PMID:11885030 PMID:12325019 PMID:12843318 PMID:14598336 PMID:20301670 PMID:21831886 PMID:24328834 PMID:25473036 PMID:25741868 PMID:26350204 PMID:26418480 PMID:27465203 PMID:27781091 PMID:27929079 PMID:28492532 PMID:32581362


  • An association has been curated linking MECP2 and Neurodevelopmental Disorders 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:9480885 (Homo sapiens)
  • 13563 RGD objects have been annotated to Neurodevelopmental Disorders  (DOID:9004429)
  • 23 papers in RGD have been used to annotate MECP2
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder
  • Original References(s): PMID:10767337 PMID:10991688 PMID:11055848 PMID:11055898 PMID:14649554 PMID:15057977 PMID:16473305 PMID:18414213 PMID:23696494 PMID:23770565 PMID:23921973 PMID:24511209 PMID:24970834 PMID:25741868 PMID:28492532 PMID:34837432


  • Go Back to source page   Continue to Ontology report