TNF Superfamily - Human Ligand-Receptor Interactions and their Associated Functions

Pathway network for the TNF Superfamily - Human Ligand-Receptor Interactions and their Associated Functions SuperPath

Sources:
  • R&D Systems
  • QIAGEN
  • Reactome

Pathways in the TNF Superfamily - Human Ligand-Receptor Interactions and their Associated Functions SuperPath

#NameSourceGenes
1TNF Superfamily - Human Ligand-Receptor Interactions and their Associated FunctionsR&D Systems
2TNF Superfamily PathwayQIAGEN
3TRAF PathwayQIAGEN
414-3-3 Induced ApoptosisQIAGEN
5TNFs bind their physiological receptorsReactome

Gene overlap in member pathways for TNF Superfamily - Human Ligand-Receptor Interactions and their Associated Functions SuperPath

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

Disorders associated with TNF Superfamily - Human Ligand-Receptor Interactions and their Associated Functions SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Tooth agenesisEnrichmentEDA, EDA2R, EDAR, EDARADD6.98
2Autoimmune lymphoproliferative syndromeEnrichmentCASP10, FAS, FASLG5.86
3Ectodermal dysplasia 1, hypohidrotic, x-linkedEnrichmentEDA, EDA2R5.39
4Common variable immunodeficiencyEnrichmentCD40LG, NFKB1, TNFRSF13B5.01
5Multisystem inflammatory syndrome in childrenEnrichmentIRAK3, TLR3, TLR6, TRAF34.92
6Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessiveEnrichmentEDAR, EDARADD4.91
7Paget disease of bone 5, juvenile-onsetEnrichmentTNFRSF11A, TNFRSF11B4.84
8Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessiveEnrichmentEDA, EDAR4.61
9Ectodermal dysplasiaEnrichmentEDA, EDAR4.61
10Immunodeficiency 33EnrichmentIKBKG, IRAK44.44
11Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA4.44
12Transient predisposition to invasive pyogenic bacterial infectionEnrichmentIRAK4, MYD884.44
13Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentEDAR, EDARADD4.39
14Autosomal recessive hypohidrotic ectodermal dysplasia syndromeEnrichmentEDAR, EDARADD4.39
15Psoriatic arthritisEnrichmentLTA, TNF4.37
16Systemic lupus erythematosusEnrichmentIRAK1, TNF, TNFAIP3, TNIP14.06
17Tooth agenesis, selective, 1EnrichmentEDA, EDA2R3.83
18Behcet syndromeEnrichmentIL12A, TLR4, TNFRSF1A3.60
19Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K23.53
20Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K23.53
21Herpes simplex virus encephalitisEnrichmentTLR3, TRAF33.37
22MalariaEnrichmentIKBKG, TIRAP, TNF3.34
23Myocardial infarctionEnrichmentLTA, TNFSF43.03
24Alzheimer's diseaseEnrichmentAPP, TNF2.96
25Ellis-van creveld syndromeEnrichmentPRKACA, PRKACB2.90
26Lung cancerEnrichmentCASP8, FAS, FASLG2.83
27Specific learning disabilityEnrichmentMAPK1, YWHAG2.72
28Immune deficiency, familial variableEnrichmentTNFRSF13B2.69
29Leprosy 4EnrichmentLTA2.69
30Immunodeficiency 16EnrichmentTNFRSF42.69
31Lymphoproliferative syndrome 3EnrichmentCD702.69
32Tooth agenesis, selective, x-linked, 1EnrichmentEDA2.69
33Immunoglobulin a deficiency 2EnrichmentTNFRSF13B2.69
34Hair morphology 1EnrichmentEDAR2.69
35Ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominantEnrichmentEDARADD2.69
36Immunodeficiency 109 with lymphoproliferationEnrichmentTNFRSF92.69
37Common variable immunodeficiency phenotype due to homozygous taci deficiencyEnrichmentTNFRSF13B2.69
38Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.42
39Osteopetrosis, autosomal recessive 7EnrichmentTNFRSF11A2.42
40Immunodeficiency with hyper-igm, type 1EnrichmentCD40LG2.42
41Immunodeficiency with hyper-igm, type 3EnrichmentCD402.42
42Cerebral amyloid angiopathy, app-relatedEnrichmentAPP2.42
43Glaucoma 1, open angle, oEnrichmentNTF42.42
44Multiple sclerosis 5EnrichmentTNFRSF1A2.42
45Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.42
46Amelogenesis imperfecta, type iiicEnrichmentRELT2.42
47Cd40 ligand deficiencyEnrichmentCD40LG2.42
48Common variable immunodeficiency phenotype due to tweak deficiencyEnrichmentTNFSF122.42
49Immunodeficiency, common variable, 2EnrichmentTNFRSF13B2.38
50Immunodeficiency with hyper-igm, type 2EnrichmentTNFRSF13B2.38
51Osteopetrosis, autosomal recessive 2EnrichmentTNFSF112.38
52Noonan syndrome and noonan-related syndromeEnrichmentMAP2K1, MAP2K22.31
53Proteus syndromeEnrichmentAKT12.22
54Acrodysostosis 1 with or without hormone resistanceEnrichmentPRKAR1A2.22
55Incontinentia pigmentiEnrichmentIKBKG2.22
56Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.22
57Immunodeficiency 68EnrichmentMYD882.22
58Caspase 8 deficiencyEnrichmentCASP82.22
59Carney complex, type 1EnrichmentPRKAR1A2.22
60Macroglobulinemia, waldenstrom 1EnrichmentMYD882.22
61Fetal encasement syndromeEnrichmentCHUK2.22
62Ataxia-oculomotor apraxia 3EnrichmentPIK3R52.22
63Immunodeficiency 15bEnrichmentIKBKB2.22
64Noonan syndrome 13EnrichmentMAPK12.22
65Immunodeficiency 15aEnrichmentIKBKB2.22
66Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.22
67Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.22
68Short syndromeEnrichmentPIK3R12.22
69Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.22
70Cardioacrofacial dysplasia 2EnrichmentPRKACB2.22
71Myxoma, intracardiacEnrichmentPRKAR1A2.22
72Chronic recurrent multifocal osteomyelitis 3EnrichmentIL1R12.22
73Asthma-related traits 5EnrichmentIRAK32.22
74Thrombocytopenia 4EnrichmentCYCS2.22
75Autoimmune lymphoproliferative syndrome, type iiaEnrichmentCASP102.22
76Immunodeficiency 67EnrichmentIRAK42.22
77Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.22
78Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD2.22
79Cowden syndrome 6EnrichmentAKT12.22
80Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.22
81Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.22
82Macular degeneration, age-related, 10EnrichmentTLR42.22
83Developmental and epileptic encephalopathy 56EnrichmentYWHAG2.22
84Cardioacrofacial dysplasia 1EnrichmentPRKACA2.22
85Bartsocas-papas syndrome 2EnrichmentCHUK2.22
86Intellectual developmental disorder, autosomal recessive 80, with variant lissencephalyEnrichmentCASP22.22
87Familial behcet-like autoinflammatory syndromeEnrichmentTNFAIP32.22
88Immunodeficiency 112EnrichmentMAP3K142.22
89Prkar1b-related neurodegenerative dementia with intermediate filamentsEnrichmentPRKAR1B2.22
90Waldenstram macroglobulinemiaEnrichmentMYD882.22
91Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.22
92Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.22
93Nik deficiencyEnrichmentMAP3K142.22
94Mycosis fungoidesEnrichmentTNFRSF1B2.21
95Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG2.21
96Tooth agenesis, selective, 2EnrichmentEDA2.21
97Saczary syndromeEnrichmentTNFRSF1B2.21
98Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.18
99Leprosy 3EnrichmentTLR22.18
100Legionnaire diseaseEnrichmentTLR52.18
101Immunodeficiency 83 viral infectionsEnrichmentTLR32.18
102Bacteremia 1EnrichmentTIRAP2.18
103Leprosy 5EnrichmentTLR12.18
104Frontometaphyseal dysplasia 2EnrichmentMAP3K72.18
105Immunodeficiency 74, covid19-related, x-linkedEnrichmentTLR72.18
106Systemic lupus erythematosus 1EnrichmentTLR52.18
107X-linked immunodeficiency 74EnrichmentTLR72.18
108Immunodeficiency 132aEnrichmentTRAF32.18
109Immunodeficiency 132bEnrichmentTRAF32.18
110Systemic lupus erythematosus 17EnrichmentTLR72.18
111Deeah syndromeEnrichmentMADD2.18
112Immunodeficiency 29EnrichmentIL12B2.18
113MelioidosisEnrichmentTLR52.18
114Thrombocytopenia 6EnrichmentSRC2.18
115Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.18
116Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotoniaEnrichmentMADD2.18
117Polyvalvular heart disease syndromeEnrichmentTAB22.18
118Melorheostosis, isolatedEnrichmentMAP2K12.15
119Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.15
120MelorheostosisEnrichmentMAP2K12.15
121Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.15
122Cerebral amyloid angiopathy, cst3-relatedEnrichmentAPP2.12
123Familial expansile osteolysisEnrichmentTNFRSF11A2.12
124Immunodeficiency 127EnrichmentTNF2.12
125Immunodeficiency, common variable, 4EnrichmentTNFRSF13C2.12
126Intermittent hydrarthrosisEnrichmentTNFRSF1A2.12
127Immunodeficiency, common variable, 1EnrichmentTNFRSF13B2.08
128Lymphoproliferative syndrome 2EnrichmentCD272.08
129Chondrocalcinosis 2EnrichmentTNFRSF11B2.08
130Autosomal recessive osteopetrosisEnrichmentTNFSF112.08
131Breast cancerEnrichmentAKT1, CASP8, JUN1.98
132Noonan syndrome 1EnrichmentMAP2K1, MAP2K21.94
133DysosteosclerosisEnrichmentTNFRSF11A1.94
134Migraine without auraEnrichmentTNF1.94
135Laryngeal squamous cell carcinomaEnrichmentTNFRSF10B1.94
136Adult-onset myasthenia gravisEnrichmentTNFRSF11A1.94
137Vogt-koyanagi-harada diseaseEnrichmentFAS1.94
138Scoliosis, isolated 1EnrichmentMAPK71.92
139Amelogenesis imperfecta, type igEnrichmentPRKAR1A1.92
140Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2EnrichmentPIK3R51.92
141Pigmented nodular adrenocortical disease, primary, 1EnrichmentPRKAR1A1.92
142Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA1.92
143Bleeding disorder, platelet-type, 19EnrichmentPRKACG1.92
144Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB11.92
145Autoinflammatory syndrome, familial, behcet-like 1EnrichmentTNFAIP31.92
146Marbach-schaaf neurodevelopmental syndromeEnrichmentPRKAR1B1.92
147Usher syndrome, type ivEnrichmentPRKAR1A1.92
148Intravascular large b-cell lymphomaEnrichmentBCL21.92
149AcrodysostosisEnrichmentPRKAR1A1.92
150Congenital dyserythropoietic anemiaEnrichmentIRAK41.92
151Fibrolamellar carcinomaEnrichmentPRKACA1.92
152Ciliary dyskinesia, primary, 18EnrichmentPRKAR1B1.92
153Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG1.92
154Isolated primary pigmented nodular adrenocortical diseaseEnrichmentPRKAR1A1.92
155Common variable immunodeficiency 12EnrichmentNFKB11.92
156Oculootodental syndromeEnrichmentFADD1.92
157Leprosy 1EnrichmentTLR61.88
158Congenital heart defects, multiple types, 2EnrichmentTAB21.88
159Immunodeficiency 57 with autoinflammationEnrichmentRIPK11.88
160Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB21.88
161Submucosal cleft palateEnrichmentUBB1.88
162Cleft hard palateEnrichmentUBB1.88
163Tafro syndromeEnrichmentMAP2K21.85
164Mitochondrial dna depletion syndrome 4aEnrichmentEDAR1.84
165RasopathyEnrichmentMAP2K1, MAP2K21.84
166Paget disease of bone 2, early-onsetEnrichmentTNFRSF11A1.82
167Paget's disease of bone 2EnrichmentTNFRSF11A1.82
168Cerebral malariaEnrichmentTNF1.82
169Narcolepsy 1EnrichmentTNFSF41.79
170Mitochondrial dna depletion syndrome 4bEnrichmentEDAR1.79
171Nasopharyngeal carcinomaEnrichmentNFKBIA1.74
172Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3R11.74
173Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R11.74
174Miller-dieker lissencephaly syndromeEnrichmentYWHAE1.74
175Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE1.74
176High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL21.74
177Immunodeficiency 14EnrichmentPIK3R11.74
178Primary biliary cholangitisEnrichmentTNFSF151.73
179Vascular dementiaEnrichmentTNF1.72
180Pelvic organ prolapseEnrichmentTAB21.70
181Takayasu arteritisEnrichmentIL12B1.70
182Uvula, bifidEnrichmentUBB1.70
183Cleft soft palateEnrichmentUBB1.70
184Frontometaphyseal dysplasiaEnrichmentMAP3K71.70
185Colorectal cancerEnrichmentPIK3R1, SRC, TLR21.70
186Langerhans cell histiocytosisEnrichmentMAP2K11.68
187Immune deficiency diseaseEnrichmentCD271.65
188Combined immunodeficiencyEnrichmentCD271.65
189Combined t cell and b cell immunodeficiencyEnrichmentCD271.65
190Combined t and b cell immunodeficiencyEnrichmentCD271.65
191Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndromeEnrichmentBDNF1.64
192Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3R21.62
193Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.62
194Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R21.62
195Carney complex variantEnrichmentPRKAR1A1.62
196Arrhythmogenic right ventricular dysplasia, familial, 10EnrichmentPRKAR1A1.62
197Congenital generalized lipodystrophyEnrichmentFOS1.62
198Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentYWHAZ1.62
199Pediatric systemic lupus erythematosusEnrichmentIRAK11.62
200Anemia, autoimmune hemolyticEnrichmentTLR81.58
201Squamous cell carcinoma, head and neckEnrichmentTNFRSF10B1.58
202Neuropathy, hereditary sensory and autonomic, type vEnrichmentNGF1.58
203Alzheimer's disease 1EnrichmentAPP1.58
204Early-onset autosomal dominant alzheimer diseaseEnrichmentAPP1.58
205Gastric cancerEnrichmentCASP10, IL1B1.56
206Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.55
207Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.52
208Follicular lymphomaEnrichmentBCL21.52
209Histiocytoid hemangiomaEnrichmentFOS1.52
210Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.52
211Endometrial stromal sarcomaEnrichmentYWHAE1.52
212Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC31.48
213Multiple acyl-coa dehydrogenase deficiency, severe neonatal typeEnrichmentMADD1.48
214Charge syndromeEnrichmentTNFRSF1A1.47
215Congenital central hypoventilation syndromeEnrichmentBDNF1.47
216Adrenocortical carcinomaEnrichmentPRKAR1A1.45
217Breast adenocarcinomaEnrichmentAKT11.45
218Kidney clear cell sarcomaEnrichmentYWHAE1.45
219Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA, YWHAZ1.44
220Amelogenesis imperfecta, type ieEnrichmentRELT1.42
221Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.41
222Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.41
223AsthmaEnrichmentTNF1.38
224Overgrowth syndromeEnrichmentPIK3R11.38
225Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA, YWHAG1.35
226Multiple endocrine neoplasia, type iEnrichmentMAP4K21.34
227MyelofibrosisEnrichmentSRC1.34
228Lymphoma, non-hodgkin, familialEnrichmentCASP101.32
229Lennox-gastaut syndromeEnrichmentMAPK101.32
230Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.31
231Amelogenesis imperfectaEnrichmentRELT1.31
232Multiple sclerosisEnrichmentTNFRSF1A1.28
233Coronary heart disease 5EnrichmentIKBKG1.27
234Adult hepatocellular carcinomaEnrichmentCASP81.27
235Cowden syndromeEnrichmentAKT11.27
236Myeloma, multipleEnrichmentPIK3R2, TRAF51.27
237Rheumatoid arthritisEnrichmentTLR11.24
238Ciliary dyskinesia, primary, 3EnrichmentNFKB11.23
239Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.23
240Arteriovenous malformationEnrichmentMAP2K11.21
241Alzheimer disease, familial, 1EnrichmentAPP1.20
242Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.16
243MeningiomaEnrichmentAKT11.15
244Migraine with or without aura 1EnrichmentTAB21.15
245Lung non-small cell carcinomaEnrichmentMAP2K11.12
246Acute promyelocytic leukemiaEnrichmentPRKAR1A1.12
247Aortic valve disease 1EnrichmentTAB21.08
248Autoinflammatory diseaseEnrichmentTNFRSF1A1.05
249OsteoporosisEnrichmentSRC1.05
250GliosarcomaEnrichmentNFKBIA1.03
251Giant cell glioblastomaEnrichmentNFKBIA1.01
252Heart, malformation ofEnrichmentMAPK10.99
253Diffuse large b-cell lymphomaEnrichmentMYD880.96
254Human immunodeficiency virus type 1EnrichmentTLR30.95
255Patent foramen ovaleEnrichmentTAB20.95
256Peripheral nervous system diseaseEnrichmentNGF0.94
257NeuropathyEnrichmentNGF0.94
258Hepatocellular carcinomaEnrichmentCASP80.90
259Severe covid-19EnrichmentCASP100.79
260MicrocephalyEnrichmentMAPK1, YWHAG0.77
261Body mass index quantitative trait locus 11EnrichmentBDNF0.76
262Severe combined immunodeficiencyEnrichmentIKBKB0.74
263Hereditary breast carcinomaEnrichmentAKT10.63
264ThrombocytopeniaEnrichmentCYCS0.60
265Hereditary breast ovarian cancer syndromeEnrichmentRIPK10.51
266Primary ciliary dyskinesiaEnrichmentPRKAR1B0.43
267Dilated cardiomyopathyEnrichmentTAB20.38
268Ovarian cancerEnrichmentAKT10.34
269Autism spectrum disorderEnrichmentMAP2K10.27
270Inherited cancer-predisposing syndromeEnrichmentPRKAR1A0.26
271Complex neurodevelopmental disorderEnrichmentMADD0.25

Loading...
Loading...
Loading...