Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 GeneticVariation disease BEFREE A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene. 18097132 2007
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 GeneticVariation disease CLINVAR Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia. 17768112 2007
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 GeneticVariation disease UNIPROT Molecular characterization of a third case of human atransferrinemia. 15466165 2004
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 Biomarker disease CTD_human Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia. 12111369 2002
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 GeneticVariation disease CLINVAR Biochemical and genetic defects underlying human congenital hypotransferrinemia. 11920219 2000
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 Biomarker disease GENOMICS_ENGLAND The effect of transferrin polymorphisms on iron metabolism. 10660486 2000
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 GeneticVariation disease UNIPROT Molecular characterization of a case of atransferrinemia. 11110675 2000
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 Biomarker disease GENOMICS_ENGLAND Molecular characterization of a case of atransferrinemia. 11110675 2000
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 Biomarker disease CTD_human Molecular characterization of a case of atransferrinemia. 11110675 2000
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 Biomarker disease GENOMICS_ENGLAND Congenital atransferrinemia. A case report and review of the literature. 1862777 1991
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 Biomarker disease MGD Hereditary hypotransferrinemia with hemosiderosis, a murine disorder resembling human atransferrinemia. 3681112 1987
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 Biomarker disease HPO
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 CausalMutation disease CLINVAR
Entrez Id: 7018
Gene Symbol: TF
TF 		0.910 GermlineCausalMutation disease ORPHANET
Entrez Id: 100129696
Gene Symbol: INHCAP
INHCAP 		0.100 CausalMutation disease CLINVAR
Entrez Id: 2395
Gene Symbol: FXN
FXN 		0.010 Biomarker disease BEFREE Many of these disorders are characterized by iron overload and include relatively common diseases such as hereditary hemochromatosis, rare abnormalities of plasma protein synthesis (atransferrinemia and aceruloplasminemia), and the neuromuscular disease Friedreich ataxia. 11419690 2001