TF, transferrin, 7018

N. diseases: 168; N. variants: 74
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GeneticVariation disease BEFREE A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene. 18097132 2007
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GeneticVariation disease CLINVAR Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia. 17768112 2007
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GeneticVariation disease UNIPROT Molecular characterization of a third case of human atransferrinemia. 15466165 2004
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease CTD_human Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia. 12111369 2002
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GeneticVariation disease CLINVAR Biochemical and genetic defects underlying human congenital hypotransferrinemia. 11920219 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease GENOMICS_ENGLAND The effect of transferrin polymorphisms on iron metabolism. 10660486 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GeneticVariation disease UNIPROT Molecular characterization of a case of atransferrinemia. 11110675 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease GENOMICS_ENGLAND Molecular characterization of a case of atransferrinemia. 11110675 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease CTD_human Molecular characterization of a case of atransferrinemia. 11110675 2000
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease GENOMICS_ENGLAND Congenital atransferrinemia. A case report and review of the literature. 1862777 1991
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease MGD Hereditary hypotransferrinemia with hemosiderosis, a murine disorder resembling human atransferrinemia. 3681112 1987
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 Biomarker disease HPO
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 CausalMutation disease CLINVAR
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia
0.910 GermlineCausalMutation disease ORPHANET
CUI: C0028754
Disease: Obesity
Obesity
0.500 Biomarker disease CTD_human Orchestrated downregulation of genes involved in oxidative metabolic pathways in obese vs. lean high-fat young male consumers. 20882379 2011
CUI: C0028754
Disease: Obesity
Obesity
0.500 Biomarker disease RGD Target identification of the novel antiobesity agent tungstate in adipose tissue from obese rats. 16267817 2005
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 GeneticVariation disease BEFREE Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease. 21514009 2012
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 GeneticVariation disease BEFREE (2004); J Med Genet 41:261-265] reported that epistatic interaction between rs1049296 (rs1049296" genes_norm="7018">P589S) in the transferrin gene (TF) and rs1800562 (C282Y) in the hemochromatosis gene (HFE) results in significant association with risk for AD. 20029940 2010
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 Biomarker disease LHGDN Sugar chains of cerebrospinal fluid transferrin as a new biological marker of Alzheimer's disease. 18654083 2008
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 Biomarker disease CTD_human Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database. 17192785 2007
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 GeneticVariation disease LHGDN Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease. 15060098 2004
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 Biomarker disease CTD_human Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease. 15060098 2004
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.350 GeneticVariation disease BEFREE As several lines of evidence indicate that oxidative stress and free radical damage occur in AD, the transferrin gene (TF) has been suggested as a candidate locus for AD since it is the major transport protein for iron, which itself is a major factor in free radical generation. 11750985 2002
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.340 Biomarker disease PSYGENET The aim of this study was to investigate the possible influence of hemochromatosis gene mutations (HFE-C282Y and H63D) and transferrin gene C2 variant (TF-C2) on susceptibility to schizophrenia and schizoaffective disorder and/or age at first hospital admission. 21643746 2012
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.340 GeneticVariation disease BEFREE The aim of this study was to investigate the possible influence of hemochromatosis gene mutations (HFE-C282Y and H63D) and transferrin gene C2 variant (TF-C2) on susceptibility to schizophrenia and schizoaffective disorder and/or age at first hospital admission. 21643746 2012