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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking TRAPPC10 and NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SHORT STATURE, AND SPEECH DELAY 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:42723303 (Homo sapiens)
  • 2 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SHORT STATURE, AND SPEECH DELAY  (DOID:9008994)
  • 3 papers in RGD have been used to annotate TRAPPC10
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with microcephaly, short stature, and speech delay
  • Original References(s): PMID:30167849 PMID:35298461


    • An association has been curated linking TRAPPC10 and NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SHORT STATURE, AND SPEECH DELAY in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SHORT STATURE, AND SPEECH DELAY  (DOID:9008994)
  • 3 papers in RGD have been used to annotate TRAPPC10


    • An association has been curated linking TRAPPC10 and NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SHORT STATURE, AND SPEECH DELAY 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:329847895|RGD:329847896|RGD:401856260 (Homo sapiens) & RGD:329847895|RGD:329847896|RGD:401856260 (Homo sapiens) & RGD:329847895|RGD:329847896|RGD:401856260 (Homo sapiens)
  • 2 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SHORT STATURE, AND SPEECH DELAY  (DOID:9008994)
  • 3 papers in RGD have been used to annotate TRAPPC10
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with microcephaly, short stature, and speech delay
  • Original References(s): PMID:25741868


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