Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 65109
Gene Symbol: UPF3B
UPF3B
0.520 GeneticVariation disease BEFREE Our results demonstrate that in addition to Lujan-Fryns and FG syndromes, UPF3B protein truncation mutations can cause also nonspecific XLMR. 19238151 2010
Entrez Id: 65109
Gene Symbol: UPF3B
UPF3B
0.520 Biomarker disease CTD_human By systematically sequencing 737 genes (annotated in the Vertebrate Genome Annotation database) on the human X chromosome in 250 families with X-linked mental retardation, we identified mutations in the UPF3 regulator of nonsense transcripts homolog B (yeast) (UPF3B) leading to protein truncations in three families: two with the Lujan-Fryns phenotype and one with the FG phenotype. 17704778 2007
Entrez Id: 65109
Gene Symbol: UPF3B
UPF3B
0.520 GeneticVariation disease BEFREE By systematically sequencing 737 genes (annotated in the Vertebrate Genome Annotation database) on the human X chromosome in 250 families with X-linked mental retardation, we identified mutations in the UPF3 regulator of nonsense transcripts homolog B (yeast) (UPF3B) leading to protein truncations in three families: two with the Lujan-Fryns phenotype and one with the FG phenotype. 17704778 2007
Entrez Id: 65109
Gene Symbol: UPF3B
UPF3B
0.520 Biomarker disease GENOMICS_ENGLAND