×
Entrez Id: 3043
Gene Symbol: HBB
HBB
Splenomegaly
0.400
Biomarker
CTD_human
Loss of NRF2 function exacerbates the pathophysiology of sickle cell disease in a transgenic mouse model.
29255069 2018
×
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
Splenomegaly
0.400
Biomarker
CTD_human
Analysis of hematopathology and alteration of JAK1/STAT3/STAT5 signaling axis in experimental myelodysplastic syndrome.
27725143 2016
×
Entrez Id: 3845
Gene Symbol: KRAS
KRAS
Splenomegaly
0.400
Biomarker
CTD_human
Analysis of hematopathology and alteration of JAK1/STAT3/STAT5 signaling axis in experimental myelodysplastic syndrome.
27725143 2016
×
Entrez Id: 331
Gene Symbol: XIAP
XIAP
Splenomegaly
0.400
Biomarker
GENOMICS_ENGLAND
Clinical and genetic characteristics of XIAP deficiency in Japan.
22228567 2012
×
Entrez Id: 355
Gene Symbol: FAS
FAS
Splenomegaly
0.400
Biomarker
CTD_human
Depletion of autoreactive plasma cells and treatment of lupus nephritis in mice using CEP-33779, a novel, orally active, selective inhibitor of JAK2.
21880982 2011
×
Entrez Id: 5184
Gene Symbol: PEPD
PEPD
Splenomegaly
0.400
Biomarker
CTD_human
A nonsense mutation of PEPD in four Amish children with prolidase deficiency.
16470701 2006
×
Entrez Id: 100506658
Gene Symbol: OCLN
OCLN
Splenomegaly
0.400
Biomarker
CTD_human
The thiopurine methyltransferase genetic polymorphism is associated with thioguanine-related veno-occlusive disease of the liver in children with acute lymphoblastic leukemia.
17015055 2006
×
Entrez Id: 348
Gene Symbol: APOE
APOE
Splenomegaly
0.400
Biomarker
CTD_human
Familial splenomegaly: macrophage hypercatabolism of lipoproteins associated with apolipoprotein E mutation [apolipoprotein E (delta149 Leu)].
11095479 2000
×
Entrez Id: 348
Gene Symbol: APOE
APOE
Splenomegaly
0.400
Biomarker
HPO
×
Entrez Id: 331
Gene Symbol: XIAP
XIAP
Splenomegaly
0.400
Biomarker
HPO
×
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
Splenomegaly
0.400
Biomarker
HPO
×
Entrez Id: 355
Gene Symbol: FAS
FAS
Splenomegaly
0.400
GeneticVariation
CLINVAR
×
Entrez Id: 355
Gene Symbol: FAS
FAS
Splenomegaly
0.400
Biomarker
HPO
×
Entrez Id: 3845
Gene Symbol: KRAS
KRAS
Splenomegaly
0.400
Biomarker
HPO
×
Entrez Id: 5184
Gene Symbol: PEPD
PEPD
Splenomegaly
0.400
Biomarker
HPO
×
Entrez Id: 100506658
Gene Symbol: OCLN
OCLN
Splenomegaly
0.400
Biomarker
HPO
×
Entrez Id: 3043
Gene Symbol: HBB
HBB
Splenomegaly
0.400
Biomarker
HPO
×
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
Splenomegaly
0.300
Biomarker
CTD_human
STAT5BN642H is a driver mutation for T cell neoplasia.
29200404 2018
×
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
Splenomegaly
0.300
Biomarker
CTD_human
Loss of NRF2 function exacerbates the pathophysiology of sickle cell disease in a transgenic mouse model.
29255069 2018
×
Entrez Id: 351
Gene Symbol: APP
APP
Splenomegaly
0.300
Biomarker
CTD_human
The BET-Bromodomain Inhibitor JQ1 Reduces Inflammation and Tau Phosphorylation at Ser396 in the Brain of the 3xTg Model of Alzheimer's Disease.
27117003 2016
×
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
Splenomegaly
0.300
Biomarker
CTD_human
The BET-Bromodomain Inhibitor JQ1 Reduces Inflammation and Tau Phosphorylation at Ser396 in the Brain of the 3xTg Model of Alzheimer's Disease.
27117003 2016
×
Entrez Id: 3782
Gene Symbol: KCNN3
KCNN3
Splenomegaly
0.300
Biomarker
GENOMICS_ENGLAND
A de novo mutation in KCNN3 associated with autosomal dominant idiopathic non-cirrhotic portal hypertension.
26658685 2016
×
Entrez Id: 2122
Gene Symbol: MECOM
MECOM
Splenomegaly
0.300
Biomarker
CTD_human
Analysis of hematopathology and alteration of JAK1/STAT3/STAT5 signaling axis in experimental myelodysplastic syndrome.
27725143 2016
×
Entrez Id: 324
Gene Symbol: APC
APC
Splenomegaly
0.300
Biomarker
CTD_human
Analysis of hematopathology and alteration of JAK1/STAT3/STAT5 signaling axis in experimental myelodysplastic syndrome.
27725143 2016
×
Entrez Id: 5663
Gene Symbol: PSEN1
PSEN1
Splenomegaly
0.300
Biomarker
CTD_human
The BET-Bromodomain Inhibitor JQ1 Reduces Inflammation and Tau Phosphorylation at Ser396 in the Brain of the 3xTg Model of Alzheimer's Disease.
27117003 2016