IDO1, indoleamine 2,3-dioxygenase 1, 3620

N. diseases: 295; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7010461
rs7010461
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs10089084
rs10089084
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE Therefore, this study aimed to investigate the association between the occurrence of <i>TPH1, TPH2, KAT1, KAT2</i> and <i>IDO1</i> polymorphisms and the risk of stroke development.The following 10 polymorphisms of the genes encoding enzymes of the TRYCATs pathway were selected: c.804-7C > A (rs10488682), c.-1668T > A (rs623580), c.803+221C > A (rs1800532), c.-173A > T (rs1799913) - <i>TPH1</i>, c.-1449C > A (rs7963803), and c.-844G > T (rs4570625) - <i>TPH2</i>. c.*456G > A of <i>KAT1</i> (rs10988134), c.975-7T > C of <i>KAT2</i> (rs1480544), c.-1849C > A (rs3824259) and c. -1493G > C (rs10089084) of <i>IDO1</i>. 31817010 2019
dbSNP: rs3739319
rs3739319
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0011311
Disease:
Dengue Fever
0.010 GeneticVariation BEFREE We genotyped 193 of the dengue cases using quantitative polymerase chain reaction to the SNP rs3739319. 31194647 2019
dbSNP: rs3739319
rs3739319
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0019100
Disease:
Severe Dengue
0.010 GeneticVariation BEFREE AA <i>IDO1</i> Variant Genotype (G2431A, rs3739319) Is Associated with Severe Dengue Risk Development in a DEN-3 Brazilian Cohort. 31194647 2019
dbSNP: rs3824259
rs3824259
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE Therefore, this study aimed to investigate the association between the occurrence of <i>TPH1, TPH2, KAT1, KAT2</i> and <i>IDO1</i> polymorphisms and the risk of stroke development.The following 10 polymorphisms of the genes encoding enzymes of the TRYCATs pathway were selected: c.804-7C > A (rs10488682), c.-1668T > A (rs623580), c.803+221C > A (rs1800532), c.-173A > T (rs1799913) - <i>TPH1</i>, c.-1449C > A (rs7963803), and c.-844G > T (rs4570625) - <i>TPH2</i>. c.*456G > A of <i>KAT1</i> (rs10988134), c.975-7T > C of <i>KAT2</i> (rs1480544), c.-1849C > A (rs3824259) and c. -1493G > C (rs10089084) of <i>IDO1</i>. 31817010 2019
dbSNP: rs9657182
rs9657182
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0020179
Disease:
Huntington Disease
0.010 GeneticVariation BEFREE The rs9657182 TT genotype associates with infection-related mortality of HD patients. 29935858 2018
dbSNP: rs9657182
rs9657182
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0019829
Disease:
Hodgkin Disease
0.010 GeneticVariation BEFREE The rs9657182 TT genotype associates with infection-related mortality of HD patients. 29935858 2018
dbSNP: rs7820268
rs7820268
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0010346
Disease:
Crohn Disease
0.010 GeneticVariation BEFREE Neither a single-nucleotide polymorphism (SNP) rs7820268 in the IDO gene, nor a widely reported CD predisposing SNP ATG16L1rs2241880 modulated the suppressive function of MSCs carrying these haplotypes. 25899824 2015
dbSNP: rs7820268
rs7820268
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0036421
Disease:
Systemic Scleroderma
0.010 GeneticVariation BEFREE SNP rs7820268 was statistically more frequent in SSc patients than in controls. 23200754 2013
dbSNP: rs9657182
rs9657182
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0086132
Disease:
Depressive Symptoms
0.010 GeneticVariation BEFREE In subjects homozygous for the risk allele (CC, n=150), the odds ratio for developing moderate or severe depressive symptoms at treatment week 12 was 2.91 (confidence interval: 1.48-5.73) compared with TT homozygotes (n=270). rs9657182 did not predict depression in African Americans, who exhibited a markedly lower frequency of the risk allele at this locus. 21691274 2012
dbSNP: rs9657182
rs9657182
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0344315
Disease:
Depressed mood
0.010 GeneticVariation BEFREE In subjects homozygous for the risk allele (CC, n=150), the odds ratio for developing moderate or severe depressive symptoms at treatment week 12 was 2.91 (confidence interval: 1.48-5.73) compared with TT homozygotes (n=270). rs9657182 did not predict depression in African Americans, who exhibited a markedly lower frequency of the risk allele at this locus. 21691274 2012
dbSNP: rs9657182
rs9657182
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0011570
Disease:
Mental Depression
0.010 GeneticVariation BEFREE In subjects homozygous for the risk allele (CC, n=150), the odds ratio for developing moderate or severe depressive symptoms at treatment week 12 was 2.91 (confidence interval: 1.48-5.73) compared with TT homozygotes (n=270). rs9657182 did not predict depression in African Americans, who exhibited a markedly lower frequency of the risk allele at this locus. 21691274 2012
dbSNP: rs9657182
rs9657182
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0011581
Disease:
Depressive disorder
0.010 GeneticVariation BEFREE In subjects homozygous for the risk allele (CC, n=150), the odds ratio for developing moderate or severe depressive symptoms at treatment week 12 was 2.91 (confidence interval: 1.48-5.73) compared with TT homozygotes (n=270). rs9657182 did not predict depression in African Americans, who exhibited a markedly lower frequency of the risk allele at this locus. 21691274 2012
dbSNP: rs4613984
rs4613984
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0086543
Disease:
Cataract
0.010 GeneticVariation BEFREE It is possible that the substitution c.422+90G → A; rs4613984 in an intron downstream to exon 4 of IDO may be related with cataract formation among the aged. 21617756 2011