Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 Biomarker disease CTD_human
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.400 GeneticVariation disease CLINVAR
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.400 Biomarker disease CTD_human
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.400 CausalMutation disease CLINVAR
Entrez Id: 4566
Gene Symbol: TRNK
TRNK 		0.100 CausalMutation disease CLINVAR
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 GeneticVariation disease UNIPROT Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029 1999
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029 1999
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.100 CausalMutation disease CLINVAR Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029 1999
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. 10852545 2000
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.100 CausalMutation disease CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. 10852545 2000
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR MNGIE: diarrhea and leukoencephalopathy. 12084896 2002
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Phenotypic variability in a Spanish family with MNGIE. 12177387 2002
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 GeneticVariation disease UNIPROT Phenotypic variability in a Spanish family with MNGIE. 12177387 2002
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.100 CausalMutation disease CLINVAR Phenotypic variability in a Spanish family with MNGIE. 12177387 2002
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients. 12529715 2003
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.100 CausalMutation disease CLINVAR Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients. 12529715 2003
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes. 14720311 2004
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.100 CausalMutation disease CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes. 14720311 2004
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutation. 14757860 2004
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE. 15505189 2004
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Clinicopathological aspects of the neuropathy of neurogastrointestinal encephalomyopathy (MNGIE) in four patients including two with a Charcot-Marie-Tooth presentation. 15742109 2005
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome. 15781193 2005
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.100 CausalMutation disease CLINVAR Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome. 15781193 2005
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Late-onset MNGIE due to partial loss of thymidine phosphorylase activity. 16178026 2005