TRAIL signaling pathway

Pathway network for the TRAIL signaling pathway SuperPath

Sources:
  • PubChem
  • Reactome

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

Disorders associated with TRAIL signaling pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Autoimmune lymphoproliferative syndromeEnrichmentCASP10, FAS, FASLG7.32
2Lung cancerEnrichmentCASP8, FAS, FASLG, PIK3CA6.06
3Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.05
4Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R1, SRC4.31
5Breast adenocarcinomaEnrichmentAKT1, PIK3CA4.09
6Adult hepatocellular carcinomaEnrichmentCASP8, PIK3CA3.97
7Cowden syndromeEnrichmentAKT1, PIK3CA3.72
8Caspase 8 deficiencyEnrichmentCASP83.66
9Autoimmune lymphoproliferative syndrome, type iiaEnrichmentCASP103.66
10Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD3.66
11Immune deficiency diseaseEnrichmentRIPK1, SYK3.53
12MeningiomaEnrichmentAKT1, PIK3CA3.46
13Oculootodental syndromeEnrichmentFADD3.35
14Hepatocellular carcinomaEnrichmentCASP8, PIK3CA3.17
15Breast cancerEnrichmentAKT1, CASP8, PIK3CA3.14
16Ovarian cancerEnrichmentAKT1, MAP3K1, PIK3CA2.77
17Lymphoma, non-hodgkin, familialEnrichmentCASP102.75
18MacrodactylyEnrichmentPIK3CA2.75
19Incontinentia pigmentiEnrichmentIKBKG2.75
20Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.75
21Megalencephaly, autosomal dominantEnrichmentPIK3CA2.75
22Cowden syndrome 5EnrichmentPIK3CA2.75
23Fetal encasement syndromeEnrichmentCHUK2.75
2446,xy sex reversal 6EnrichmentMAP3K12.75
25Cerebral cavernous malformations 4EnrichmentPIK3CA2.75
26Immunodeficiency 15bEnrichmentIKBKB2.75
27Immunodeficiency 15aEnrichmentIKBKB2.75
28Short syndromeEnrichmentPIK3R12.75
29Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.75
30Hemifacial myohyperplasiaEnrichmentPIK3CA2.75
31Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.75
32Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.75
33Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.75
34Acid sphingomyelinase deficiencyEnrichmentSMPD12.75
35Bartsocas-papas syndrome 2EnrichmentCHUK2.75
36Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.75
37Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.75
38HypospadiasEnrichmentPIK3CA2.75
39Perrault syndrome 7EnrichmentDAP32.75
40Rare venous malformationEnrichmentPIK3CA2.75
41Diaphragmatic eventrationEnrichmentPIK3CA2.75
42Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.75
43Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.75
44Rare combined vascular malformationEnrichmentPIK3CA2.75
45Cavernous lymphangiomaEnrichmentPIK3CA2.75
46Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.75
47Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.75
48Eccrine angiomatous hamartomaEnrichmentPIK3CA2.75
49Macrodactyly of toeEnrichmentPIK3CA2.75
50Proteus syndromeEnrichmentAKT12.63
51Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.63
52Isolated growth hormone deficiency type iiiEnrichmentBTK2.63
53Cowden syndrome 6EnrichmentAKT12.63
54Thrombocytopenia 6EnrichmentSRC2.63
55ColitisEnrichmentSYK2.63
56Gastric cancerEnrichmentCASP10, PIK3CA2.59
57Grange syndromeEnrichmentDAP32.45
58Immunodeficiency 33EnrichmentIKBKG2.45
59Keratosis, seborrheicEnrichmentPIK3CA2.45
60Noonan syndrome 8EnrichmentPIK3CA2.45
61Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.45
62Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG2.45
63Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.45
64Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.45
65Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK2.33
66Cerebellar ataxia, neuropathy, and vestibular areflexia syndromeEnrichmentRFC12.33
67Agammaglobulinemia, x-linkedEnrichmentBTK2.33
68ArthritisEnrichmentSYK2.33
69Hereditary breast carcinomaEnrichmentAKT1, PIK3CA2.32
70Pompe disease, infantile-onsetEnrichmentPIK3CA2.28
71Niemann-pick disease, type aEnrichmentSMPD12.28
72Niemann-pick disease, type bEnrichmentSMPD12.28
73Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.28
74Ceroid lipofuscinosis, neuronal, 6aEnrichmentSMPD12.28
75Immunodeficiency 14EnrichmentPIK3R12.28
76Laryngeal squamous cell carcinomaEnrichmentTNFRSF10B2.28
77KeratoacanthomaEnrichmentPIK3CA2.28
78Severe covid-19EnrichmentCASP102.19
79Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.15
80Cerebrovascular diseaseEnrichmentPIK3CA2.15
81Familial cerebral cavernous malformationsEnrichmentPIK3CA2.15
82Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG2.15
83Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK2.15
84Intellectual developmental disorder, autosomal dominant 56EnrichmentCLTC2.15
85Agammaglobulinemia 1EnrichmentBTK2.15
86Vogt-koyanagi-harada diseaseEnrichmentFAS2.15
87Capillary malformations, congenitalEnrichmentPIK3CA2.05
88Niemann-pick disease, type c1EnrichmentSMPD12.05
89Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG2.05
90Niemann-pick diseaseEnrichmentSMPD12.05
91HemimegalencephalyEnrichmentPIK3CA2.05
92Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1EnrichmentCLTC2.03
93Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.98
94Cowden syndrome 1EnrichmentPIK3CA1.98
95Hemihyperplasia, isolatedEnrichmentPIK3CA1.98
96Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.98
97Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.98
98Lung squamous cell carcinomaEnrichmentPIK3CA1.98
99Nevus, epidermalEnrichmentPIK3CA1.91
100Squamous cell carcinoma, head and neckEnrichmentTNFRSF10B1.91
101Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.91
102Gallbladder cancerEnrichmentPIK3CA1.91
103Overgrowth syndromeEnrichmentPIK3R11.91
104Inflammatory myofibroblastic tumorEnrichmentCLTC1.85
105Coronary heart disease 5EnrichmentIKBKG1.80
106Arteriovenous malformationEnrichmentPIK3CA1.80
107MyelofibrosisEnrichmentSRC1.79
108Noonan syndrome 3EnrichmentCLTC1.79
109Renal cell carcinoma with mit translocationsEnrichmentCLTC1.79
110Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.76
111Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.76
11246,xy complete gonadal dysgenesisEnrichmentMAP3K11.71
113Lung non-small cell carcinomaEnrichmentPIK3CA1.71
114Lip and oral cavity carcinomaEnrichmentPIK3CA1.68
115Nk-cell enteropathyEnrichmentPIK3CB1.64
11646,xy partial gonadal dysgenesisEnrichmentMAP3K11.61
117Lynch syndromeEnrichmentPIK3CA1.58
118Perrault syndrome 1EnrichmentDAP31.55
119OsteoporosisEnrichmentSRC1.49
120Endometrial cancerEnrichmentPIK3CA1.44
121MalariaEnrichmentIKBKG1.40
122Behcet syndromeEnrichmentFAS1.36
123Diffuse large b-cell lymphomaEnrichmentBTK1.36
124Parkinson's diseaseEnrichmentRFC11.36
125Bladder cancerEnrichmentPIK3CA1.30
126Prostate cancerEnrichmentPIK3CA1.30
127Parkinson disease, late-onsetEnrichmentRFC11.26
128Severe combined immunodeficiencyEnrichmentIKBKB1.25
129HypertelorismEnrichmentPIK3CA1.05
130Hereditary breast ovarian cancer syndromeEnrichmentRIPK11.03
131ThrombocytopeniaEnrichmentSRC0.97
132Autosomal dominant non-syndromic intellectual disabilityEnrichmentCLTC0.95
133Undetermined early-onset epileptic encephalopathyEnrichmentCLTC0.91
134Autosomal recessive non-syndromic intellectual disabilityEnrichmentEZR0.89

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