FoxO family signaling

No Pathway Network information available for FoxO family signaling

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with FoxO family signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Primary mediastinal large b-cell lymphomaEnrichmentBCL6, XPO15.30
2Ovarian cancerEnrichmentAKT1, CDKN1B, CTNNB12.81
3Proteus syndromeEnrichmentAKT12.64
4Microvascular complications of diabetes 6EnrichmentSOD22.64
5Fetal encasement syndromeEnrichmentCHUK2.64
6Immunodeficiency 15bEnrichmentIKBKB2.64
7Brunet-wagner neurodevelopmental syndromeEnrichmentRBL22.64
8Immunodeficiency 15aEnrichmentIKBKB2.64
9Neuroendocrine tumorEnrichmentCDKN1B2.64
10AcatalasemiaEnrichmentCAT2.64
11Cowden syndrome 6EnrichmentAKT12.64
12Bartsocas-papas syndrome 2EnrichmentCHUK2.64
13Adenoid ameloblastomaEnrichmentCTNNB12.64
14Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.64
15Microcystic stromal tumorEnrichmentCTNNB12.64
16Osteopathia striata with cranial sclerosisEnrichmentCTNNB12.34
17Multiple endocrine neoplasia, type ivEnrichmentCDKN1B2.34
18Intravascular large b-cell lymphomaEnrichmentBCL62.34
19Childhood hepatocellular carcinomaEnrichmentCTNNB12.34
20Hao-fountain syndromeEnrichmentUSP72.34
21Juvenile nasopharyngeal angiofibromaEnrichmentCTNNB12.34
22TeratomaEnrichmentCTNNB12.34
23Desmoid disease, hereditaryEnrichmentCTNNB12.16
24Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG2.16
25Neurodevelopmental disorder with spastic diplegia and visual defectsEnrichmentCTNNB12.16
26Anus, imperforateEnrichmentCTNNB12.16
27Exudative vitreoretinopathy 7EnrichmentCTNNB12.16
28Desmoid tumorEnrichmentCTNNB12.16
29High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL62.16
30Glycogen storage disease iaEnrichmentG6PC12.04
31Autoimmune lymphoproliferative syndromeEnrichmentFASLG2.04
32PilomatrixomaEnrichmentCTNNB12.04
33Alazami syndromeEnrichmentCTNNB12.04
34CraniopharyngiomaEnrichmentCTNNB12.04
35Primary hyperparathyroidismEnrichmentCDKN1B2.04
36Exudative vitreoretinopathy 1EnrichmentCTNNB11.94
37Rhabdomyosarcoma 2EnrichmentFOXO11.94
38Cholangitis, primary sclerosingEnrichmentMST11.94
39Follicular lymphomaEnrichmentBCL61.94
40HypoglycemiaEnrichmentG6PC11.94
41Weyers acrofacial dysostosisEnrichmentCTNNB11.87
42Adrenocortical carcinomaEnrichmentCTNNB11.87
43Breast adenocarcinomaEnrichmentAKT11.87
44Multiple endocrine neoplasia, type iEnrichmentCDKN1B1.80
45Gallbladder cancerEnrichmentCTNNB11.80
46Colorectal cancerEnrichmentAKT1, CTNNB11.78
47Exudative vitreoretinopathyEnrichmentCTNNB11.74
48Adult hepatocellular carcinomaEnrichmentCTNNB11.69
49Cowden syndromeEnrichmentAKT11.69
50Glycogen storage diseaseEnrichmentG6PC11.60
51MeningiomaEnrichmentAKT11.57
52MedulloblastomaEnrichmentCTNNB11.50
53Polycystic liver diseaseEnrichmentCTNNB11.42
54Autosomal dominant polycystic liver diseaseEnrichmentCTNNB11.42
55Diffuse large b-cell lymphomaEnrichmentFOXO11.37
56HepatoblastomaEnrichmentCTNNB11.33
57Hepatocellular carcinomaEnrichmentCTNNB11.31
58Bladder cancerEnrichmentCTNNB11.19
59Lung cancerEnrichmentFASLG1.15
60Severe combined immunodeficiencyEnrichmentIKBKB1.14
61Hereditary breast carcinomaEnrichmentAKT11.02
62Myeloma, multipleEnrichmentSGK10.92
63Breast cancerEnrichmentAKT10.80
64Congenital nervous system abnormalityEnrichmentCTNNB10.67
65Nervous system diseaseEnrichmentCTNNB10.67
66MicrocephalyEnrichmentCTNNB10.61
67Inherited cancer-predisposing syndromeEnrichmentCDKN1B0.58

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