Death Receptor Signaling Pathway

Pathway network for the Death Receptor Signaling Pathway SuperPath

Sources:
  • Sino Biological
  • R&D Systems
  • GeneGo (Thomson Reuters)
  • Reactome

Pathways in the Death Receptor Signaling Pathway SuperPath

#NameSourceGenes
1Death Receptor Signaling PathwaySino Biological
2Apoptosis Signaling PathwayR&D Systems
3TNF Signaling PathwaySino Biological
4Apoptosis and survival Apoptotic TNF-family pathwaysGeneGo (Thomson Reuters)
5SARS-CoV-1-mediated effects on programmed cell deathReactome

Gene overlap in member pathways for Death Receptor Signaling Pathway SuperPath

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

Disorders associated with Death Receptor Signaling Pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Severe acute respiratory syndromeDirect
2Autoimmune lymphoproliferative syndromeEnrichmentCASP10, FAS, FASLG7.02
3Adult hepatocellular carcinomaEnrichmentAXIN1, CASP8, TP535.08
4Lung cancerEnrichmentCASP8, FAS, FASLG, MAP3K84.65
5Lymphoproliferative syndrome 2EnrichmentCD27, XIAP4.30
6Nasopharyngeal carcinomaEnrichmentNFKBIA, TP534.09
7Hepatocellular carcinomaEnrichmentAXIN1, CASP8, TP533.84
8Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K23.79
9Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K23.79
10Squamous cell carcinoma, head and neckEnrichmentTNFRSF10B, TP533.34
11Immune deficiency diseaseEnrichmentCD27, RIPK13.34
12Lymphoma, non-hodgkin, familialEnrichmentCASP10, TP533.22
13Specific learning disabilityEnrichmentMAPK1, YWHAG3.16
14Behcet syndromeEnrichmentFAS, TNFRSF1A2.85
15Autoinflammatory diseaseEnrichmentTNFRSF1A, XIAP2.65
16Breast cancerEnrichmentAKT1, CASP8, JUN2.60
17Noonan syndrome and noonan-related syndromeEnrichmentMAP2K1, MAP2K22.57
18Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.53
19Lymphoproliferative syndrome, x-linked, 2EnrichmentXIAP2.53
20Caspase 8 deficiencyEnrichmentCASP82.53
21Lymphoproliferative syndrome 3EnrichmentCD702.53
22Immunodeficiency 132aEnrichmentTRAF32.53
23Immunodeficiency 132bEnrichmentTRAF32.53
24Autoimmune lymphoproliferative syndrome, type iiaEnrichmentCASP102.53
25Intellectual developmental disorder, autosomal recessive 34, with variant lissencephalyEnrichmentCRADD2.53
26Multiple sclerosis 5EnrichmentTNFRSF1A2.53
27Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD2.53
28Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.53
29Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.53
30Intellectual developmental disorder, autosomal recessive 80, with variant lissencephalyEnrichmentCASP22.53
31Common variable immunodeficiency phenotype due to tweak deficiencyEnrichmentTNFSF122.53
32GliosarcomaEnrichmentNFKBIA, TP532.51
33Giant cell glioblastomaEnrichmentNFKBIA, TP532.46
34Proteus syndromeEnrichmentAKT12.44
35Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.44
3646,xy sex reversal 6EnrichmentMAP3K12.44
37Immunodeficiency 15bEnrichmentIKBKB2.44
38Noonan syndrome 13EnrichmentMAPK12.44
39Immunodeficiency 15aEnrichmentIKBKB2.44
40Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.44
41Cowden syndrome 6EnrichmentAKT12.44
42Developmental and epileptic encephalopathy 56EnrichmentYWHAG2.44
43Capillary hemangiomaEnrichmentAKT32.44
44Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.44
45Akt2-related familial partial lipodystrophyEnrichmentAKT22.44
46Oligodontia-colorectal cancer syndromeEnrichmentAXIN22.33
47Parkinson disease 13, autosomal dominantEnrichmentHTRA22.33
48Caudal duplication anomalyEnrichmentAXIN12.33
49Myoclonus, familial, 1EnrichmentNOL32.33
50Bone marrow failure syndrome 5EnrichmentTP532.33
51Papilloma of choroid plexusEnrichmentTP532.33
52Basal cell carcinoma 7EnrichmentTP532.33
53Anaplastic thyroid carcinomaEnrichmentTP532.33
54Thrombocytopenia 4EnrichmentCYCS2.33
55Charcot-marie-tooth disease, axonal, type 2fEnrichmentHSPB12.33
56Ductal carcinoma in situEnrichmentTP532.33
57Thyroid gland undifferentiated carcinomaEnrichmentTP532.33
58Craniometadiaphyseal osteosclerosis with hip dysplasiaEnrichmentAXIN12.33
59Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.33
60Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.33
61Choroid plexus cancerEnrichmentTP532.33
62Pleomorphic xanthoastrocytomaEnrichmentTP532.33
63Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephalyEnrichmentPIDD12.33
64Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.28
65Melorheostosis, isolatedEnrichmentMAP2K12.28
66Maturity-onset diabetes of the young, type 2EnrichmentGCK2.28
67Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.28
68Frontometaphyseal dysplasia 2EnrichmentMAP3K72.28
69Hyperinsulinemic hypoglycemia, familial, 3EnrichmentGCK2.28
70MelorheostosisEnrichmentMAP2K12.28
71Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.28
72Immunodeficiency 112EnrichmentMAP3K142.28
73Gestational diabetesEnrichmentGCK2.28
74Cerebral cavernous malformations 5EnrichmentMAP3K32.28
75Verrucous hemangiomaEnrichmentMAP3K32.28
76Nik deficiencyEnrichmentMAP3K142.28
77Deafness, autosomal dominant 64EnrichmentDIABLO2.23
78Intravascular large b-cell lymphomaEnrichmentBCL22.23
79Immunodeficiency 127EnrichmentTNF2.23
80Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.23
81Intermittent hydrarthrosisEnrichmentTNFRSF1A2.23
82Oculootodental syndromeEnrichmentFADD2.23
83Noonan syndrome 1EnrichmentMAP2K1, MAP2K22.20
84Scoliosis, isolated 1EnrichmentMAPK72.14
85Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.14
86Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.14
87Rela fusion-positive ependymomaEnrichmentRELA2.14
88Senior-loken syndrome 7EnrichmentAKT32.14
89Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.14
90Bardet-biedl syndrome 16EnrichmentAKT32.14
91Colorectal cancerEnrichmentAXIN2, BAX, TP532.10
92RasopathyEnrichmentMAP2K1, MAP2K22.09
93Bladder cancerEnrichmentCDKN1A, TP532.09
94Mycosis fungoidesEnrichmentTNFRSF1B2.05
95Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG2.05
96Psoriatic arthritisEnrichmentTNF2.05
97High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL22.05
98T-cell acute lymphoblastic leukemiaEnrichmentBAX2.05
99Migraine without auraEnrichmentTNF2.05
100Laryngeal squamous cell carcinomaEnrichmentTNFRSF10B2.05
101Vogt-koyanagi-harada diseaseEnrichmentFAS2.05
102Saczary syndromeEnrichmentTNFRSF1B2.05
103Adrenocortical carcinoma, hereditaryEnrichmentTP532.03
104Spondyloepimetaphyseal dysplasia, x-linked, with hypomyelinating leukodystrophyEnrichmentAIFM12.03
105Charcot-marie-tooth disease, x-linked recessive, 4, with or without cerebellar ataxiaEnrichmentAIFM12.03
106Combined oxidative phosphorylation deficiency 6EnrichmentAIFM12.03
107Cervical cancerEnrichmentTP532.03
108Neuronopathy, distal hereditary motor, autosomal dominant 3EnrichmentHSPB12.03
109Lymphoma, hodgkin, classicEnrichmentTP532.03
110Congenital fibrosarcomaEnrichmentTP532.03
111Li-fraumeni syndrome 1EnrichmentTP532.03
112SarcomaEnrichmentTP532.03
113Cervix carcinomaEnrichmentTP532.03
114Hodgkin's lymphomaEnrichmentTP532.03
115Charcot-marie-tooth disease x-linked recessive 4EnrichmentAIFM12.03
116Pleomorphic rhabdomyosarcomaEnrichmentTP532.03
117Maturity-onset diabetes of the young, type 1EnrichmentGCK1.98
118Diabetes mellitus, permanent neonatal, 1EnrichmentGCK1.98
119Bone marrow failure syndrome 2EnrichmentGCK1.98
120Tafro syndromeEnrichmentMAP2K21.98
121Miller-dieker lissencephaly syndromeEnrichmentYWHAE1.97
122Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE1.97
123Cerebral malariaEnrichmentTNF1.93
124Spinal muscular atrophy, type iiiEnrichmentNAIP1.85
125Spinal muscular atrophy, type iEnrichmentNAIP1.85
126Spinal muscular atrophy, type iiEnrichmentNAIP1.85
127Osteogenic sarcomaEnrichmentTP531.85
128Deafness, x-linked 5, with peripheral neuropathyEnrichmentAIFM11.85
129X-linked deafness 5EnrichmentAIFM11.85
130Atypical teratoid rhabdoid tumorEnrichmentTP531.85
131Anaplastic astrocytomaEnrichmentTP531.85
132Squamous cell carcinomaEnrichmentTP531.85
133AdenocarcinomaEnrichmentTP531.85
134Combined oxidative phosphorylation deficiencyEnrichmentAIFM11.85
135Bone osteosarcomaEnrichmentTP531.85
136Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT31.84
137Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.84
138Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT31.84
139Congenital generalized lipodystrophyEnrichmentFOS1.84
140Follicular lymphomaEnrichmentBCL21.83
141Vascular dementiaEnrichmentTNF1.83
142Herpes simplex virus encephalitisEnrichmentTRAF31.83
143Nijmegen breakage syndromeEnrichmentGCK1.81
144Langerhans cell histiocytosisEnrichmentMAP2K11.81
145Frontometaphyseal dysplasiaEnrichmentMAP3K71.81
146Gastric cancerEnrichmentCASP10, TP531.76
147Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.76
148Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.76
149Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC31.75
150Histiocytoid hemangiomaEnrichmentFOS1.75
151HemimegalencephalyEnrichmentAKT31.75
152Endometrial stromal sarcomaEnrichmentYWHAE1.75
153Small cell cancer of the lungEnrichmentTP531.73
154Thyroid cancer, nonmedullary, 1EnrichmentTP531.73
155Lung sarcomatoid carcinomaEnrichmentTP531.73
156Embryonal rhabdomyosarcomaEnrichmentTP531.73
157Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentYWHAZ1.73
1583-methylglutaconic aciduria, type viiiEnrichmentHTRA21.73
159Neuropathy, hereditary sensory and autonomic, type vEnrichmentNGF1.69
160Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.68
161Maturity-onset diabetes of the young, type 3EnrichmentGCK1.68
162Breast adenocarcinomaEnrichmentAKT11.67
163Kidney clear cell sarcomaEnrichmentYWHAE1.67
164Neuronopathy, distal hereditary motor, autosomal dominant 2EnrichmentHSPB11.63
165Rhabdomyosarcoma 2EnrichmentTP531.63
166LymphomaEnrichmentTP531.63
167Acute megakaryocytic leukemiaEnrichmentTP531.63
168Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.63
169MegacolonEnrichmentAKT31.60
170Charge syndromeEnrichmentTNFRSF1A1.58
171Familial isolated arrhythmogenic right ventricular dysplasiaEnrichmentCRADD1.58
172Hereditary breast ovarian cancer syndromeEnrichmentRIPK1, TP531.56
173Li-fraumeni syndromeEnrichmentTP531.55
174Adrenocortical carcinomaEnrichmentTP531.55
175Hyperinsulinemic hypoglycemia, familial, 1EnrichmentGCK1.51
176Nonsyndromic genetic hyperinsulinismEnrichmentGCK1.51
177AsthmaEnrichmentTNF1.50
178Combined immunodeficiencyEnrichmentCD271.50
179Combined t cell and b cell immunodeficiencyEnrichmentCD271.50
180Combined t and b cell immunodeficiencyEnrichmentCD271.50
181Cowden syndromeEnrichmentAKT11.49
182Esophageal cancerEnrichmentTP531.49
183Multiple endocrine neoplasia, type iEnrichmentCDKN1A1.49
184Essential thrombocythemiaEnrichmentTP531.49
185Gallbladder cancerEnrichmentTP531.49
186B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.49
187PolymicrogyriaEnrichmentAKT31.45
188Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.44
189Glioma susceptibility 1EnrichmentTP531.43
190Alzheimer's diseaseEnrichmentTNF1.42
19146,xy complete gonadal dysgenesisEnrichmentMAP3K11.41
192Multiple sclerosisEnrichmentTNFRSF1A1.39
193Permanent neonatal diabetes mellitusEnrichmentGCK1.39
194Tooth agenesis, selective, 1EnrichmentAXIN21.38
195Primary hyperaldosteronismEnrichmentTP531.38
196Primary biliary cholangitisEnrichmentTNFSF151.38
197MeningiomaEnrichmentAKT11.37
198Arteriovenous malformationEnrichmentMAP2K11.34
199Leukemia, chronic lymphocyticEnrichmentTP531.34
200Familial colorectal cancerEnrichmentTP531.34
20146,xy partial gonadal dysgenesisEnrichmentMAP3K11.31
202Myelodysplastic syndromeEnrichmentTP531.29
203Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.29
204Ovarian cancerEnrichmentAKT1, MAP3K11.29
205Early-onset parkinson's diseaseEnrichmentHTRA21.26
206Lip and oral cavity carcinomaEnrichmentTP531.26
207Lung non-small cell carcinomaEnrichmentMAP2K11.25
208Diabetes mellitusEnrichmentGCK1.25
209Multisystem inflammatory syndrome in childrenEnrichmentTRAF31.20
210Heart, malformation ofEnrichmentMAPK11.20
211Lung cancer susceptibility 3EnrichmentTP531.19
212MalariaEnrichmentTNF1.18
213MicrocephalyEnrichmentMAPK1, YWHAG1.14
214RhabdomyosarcomaEnrichmentTP531.14
215Severe covid-19EnrichmentCASP101.09
216Diffuse large b-cell lymphomaEnrichmentTP531.07
217Peripheral nervous system diseaseEnrichmentNGF1.04
218NeuropathyEnrichmentNGF1.04
219LeukodystrophyEnrichmentAIFM11.04
220HepatoblastomaEnrichmentTP531.02
221Tooth agenesisEnrichmentAXIN21.00
222Maturity-onset diabetes of the youngEnrichmentGCK1.00
223Diamond-blackfan anemia 1EnrichmentTP530.99
224Ear malformationEnrichmentAIFM10.97
225Systemic lupus erythematosusEnrichmentTNF0.96
226Pancreatic cancerEnrichmentTP530.95
227Severe combined immunodeficiencyEnrichmentIKBKB0.95
228Auditory neuropathyEnrichmentAIFM10.94
229Hirschsprung disease 1EnrichmentAXIN20.89
230Prostate cancerEnrichmentTP530.89
231Inherited cancer-predisposing syndromeEnrichmentAXIN2, TP530.89
232Type 2 diabetes mellitusEnrichmentAKT20.85
233Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentDIABLO0.85
234Hereditary breast carcinomaEnrichmentAKT10.83
235Diamond-blackfan anemiaEnrichmentTP530.80
236Autosomal recessive non-syndromic intellectual disabilityEnrichmentCRADD0.80
237Leukemia, acute myeloidEnrichmentTP530.76
238Charcot-marie-tooth diseaseEnrichmentHSPB10.75
239Undetermined early-onset epileptic encephalopathyEnrichmentYWHAG0.74
240Sensorineural hearing lossEnrichmentAIFM10.69
241ThrombocytopeniaEnrichmentCYCS0.69
242Autosomal dominant non-syndromic intellectual disabilityEnrichmentYWHAZ0.68
243Myeloma, multipleEnrichmentTP530.63
244SchizophreniaEnrichmentBIRC60.61
245Autism spectrum disorderEnrichmentMAP2K10.36

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