Gene: DPYD ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1806
Gene Symbol: DPYD
DPYD 		0.340 GeneticVariation disease BEFREE Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder. 21114665 2011
Entrez Id: 1806
Gene Symbol: DPYD
DPYD 		0.340 GeneticVariation disease BEFREE Hemizygous DPYD deletions were previously suggested to contribute to a phenotype with autism spectrum disorder and speech delay. 22003227 2011
Entrez Id: 1806
Gene Symbol: DPYD
DPYD 		0.340 GeneticVariation disease BEFREE Two of the ASD individuals with missense changes also carried a de novo deletion at another ASD susceptibility locus (DPYD and DPP6), suggesting complex genetic contributions. 20844286 2010
Entrez Id: 1806
Gene Symbol: DPYD
DPYD 		0.340 Biomarker disease CTD_human Two of the ASD individuals with missense changes also carried a de novo deletion at another ASD susceptibility locus (DPYD and DPP6), suggesting complex genetic contributions. 20844286 2010
Entrez Id: 1806
Gene Symbol: DPYD
DPYD 		0.340 Biomarker disease BEFREE Notwithstanding complexities, our results further implicate the SHANK3-NLGN4-NRXN1 postsynaptic density genes and also identify novel loci at DPP6-DPP10-PCDH9 (synapse complex), ANKRD11, DPYD, PTCHD1, 15q24, among others, for a role in ASD susceptibility. 18252227 2008
Entrez Id: 1806
Gene Symbol: DPYD
DPYD 		0.340 Biomarker disease CTD_human Notwithstanding complexities, our results further implicate the SHANK3-NLGN4-NRXN1 postsynaptic density genes and also identify novel loci at DPP6-DPP10-PCDH9 (synapse complex), ANKRD11, DPYD, PTCHD1, 15q24, among others, for a role in ASD susceptibility. 18252227 2008