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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking SETD2 and Luscan-Lumish Syndrome in Canis lupus familiaris.        

  • 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 SETD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Luscan-Lumish Syndrome  (DOID:9008051)
  • 0 papers in RGD have been used to annotate SETD2


    • An association has been curated linking SETD2 and Luscan-Lumish Syndrome in Canis lupus familiaris.        

  • 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 SETD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Luscan-Lumish Syndrome  (DOID:9008051)
  • 0 papers in RGD have been used to annotate SETD2
  • Curation Notes: ClinVar Annotator: match by term: Luscan-Lumish syndrome | ClinVar Annotator: match by term: Luscan-lumish syndrome | ClinVar Annotator: match by term: SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth
  • Original References(s): PMID:17576681 PMID:20864444 PMID:22495309 PMID:23160955 PMID:24142049 PMID:24267886 PMID:24728327 PMID:24852293 PMID:24901346 PMID:25574603 PMID:25741868 PMID:26084711 PMID:26467025 PMID:26580448 PMID:27317772 PMID:27455002 PMID:27528607 PMID:28166811 PMID:28424246 PMID:28492532 PMID:28577310 PMID:29276005 PMID:29681085 PMID:30419952 PMID:31474318 PMID:32668055 PMID:32710489 PMID:33004838 PMID:33921431 PMID:36474027 PMID:37025455 PMID:37372360 PMID:9536098


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