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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking FOXG1 and Rett Syndrome, Congenital Variant 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 FOXG1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rett Syndrome, Congenital Variant  (DOID:9008979)
  • 0 papers in RGD have been used to annotate FOXG1


    • An association has been curated linking FOXG1 and Rett Syndrome, Congenital Variant 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 FOXG1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rett Syndrome, Congenital Variant  (DOID:9008979)
  • 0 papers in RGD have been used to annotate FOXG1
  • Curation Notes: ClinVar Annotator: match by term: FOXG1 disorder | ClinVar Annotator: match by term: FOXG1-related condition | ClinVar Annotator: match by term: Rett syndrome, congenital variant
  • Original References(s): PMID:10369754 PMID:18414213 PMID:18571142 PMID:19564653 PMID:19578037 PMID:19623215 PMID:19806373 PMID:20734096 PMID:21270142 PMID:21280142 PMID:21441262 PMID:21488007 PMID:21694734 PMID:22091895 PMID:22129046 PMID:22190898 PMID:22258524 PMID:22739344 PMID:22968132 PMID:23757202 PMID:23838309 PMID:24412290 PMID:24731847 PMID:24836831 PMID:24901346 PMID:25326635 PMID:25356899 PMID:25741868 PMID:25914188 PMID:26344814 PMID:26364767 PMID:26467025 PMID:26544041 PMID:26633542 PMID:26938784 PMID:26993267 PMID:27001178 PMID:27029630 PMID:28333917 PMID:28492532 PMID:28554332 PMID:28628100 PMID:28661489 PMID:28708303 PMID:28781028 PMID:28851325 PMID:28947817 PMID:29389947 PMID:29611406 PMID:29655203 PMID:29852413 PMID:30214071 PMID:30525188 PMID:30533527 PMID:30792901 PMID:30842224 PMID:30866059 PMID:31199603 PMID:31780880 PMID:32581362 PMID:34284163 PMID:34837432 PMID:35163265


    • An association has been curated linking FOXG1 and Rett Syndrome, Congenital Variant 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 FOXG1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rett Syndrome, Congenital Variant  (DOID:9008979)
  • 0 papers in RGD have been used to annotate FOXG1
  • Curation Notes: ClinVar Annotator: match by term: Rett syndrome, congenital variant
  • Original References(s): PMID:18414213 PMID:18571142 PMID:19564653 PMID:19578037 PMID:19623215 PMID:19806373 PMID:20734096 PMID:21270142 PMID:21280142 PMID:21441262 PMID:21488007 PMID:21694734 PMID:22091895 PMID:22129046 PMID:22190898 PMID:22258524 PMID:22739344 PMID:22968132 PMID:23757202 PMID:23838309 PMID:24412290 PMID:24731847 PMID:24836831 PMID:24901346 PMID:25326635 PMID:25356899 PMID:25741868 PMID:25914188 PMID:26344814 PMID:26364767 PMID:26467025 PMID:26633542 PMID:26938784 PMID:26993267 PMID:27001178 PMID:27029630 PMID:28492532 PMID:28554332 PMID:28628100 PMID:28661489 PMID:28708303 PMID:28781028 PMID:28851325 PMID:28947817 PMID:29389947 PMID:29611406 PMID:29655203 PMID:29852413 PMID:30525188 PMID:30533527 PMID:30792901 PMID:30842224 PMID:30866059 PMID:31780880 PMID:32581362 PMID:34284163 PMID:34837432


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