Apoptosis and survival Anti-apoptotic TNFs/NF-kB/Bcl-2 pathway

No Pathway Network information available for Apoptosis and survival Anti-apoptotic TNFs/NF-kB/Bcl-2 pathway

Pathways in the Apoptosis and survival Anti-apoptotic TNFs/NF-kB/Bcl-2 pathway SuperPath

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

Disorders associated with Apoptosis and survival Anti-apoptotic TNFs/NF-kB/Bcl-2 pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Common variable immunodeficiencyEnrichmentCD40LG, NFKB1, NFKB2, TNFRSF13B8.56
2Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA5.30
3Immunodeficiency, common variable, 1EnrichmentNFKB2, TNFRSF13B4.52
4Paget disease of bone 2, early-onsetEnrichmentSQSTM1, TNFRSF11A4.25
5Paget's disease of bone 2EnrichmentSQSTM1, TNFRSF11A4.25
6Systemic lupus erythematosusEnrichmentIRAK1, TNF, TNFSF43.63
7MalariaEnrichmentIKBKG, TNF2.91
8Autoinflammatory diseaseEnrichmentTNFRSF1A, XIAP2.87
9Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.64
10Immune deficiency, familial variableEnrichmentTNFRSF13B2.64
11Incontinentia pigmentiEnrichmentIKBKG2.64
12Lymphoproliferative syndrome, x-linked, 2EnrichmentXIAP2.64
13Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.64
14Fetal encasement syndromeEnrichmentCHUK2.64
15Immunodeficiency 15bEnrichmentIKBKB2.64
16Immunodeficiency 15aEnrichmentIKBKB2.64
17Immunodeficiency 92EnrichmentREL2.64
18Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.64
19Immunodeficiency 132aEnrichmentTRAF32.64
20Immunodeficiency 132bEnrichmentTRAF32.64
21Immunoglobulin a deficiency 2EnrichmentTNFRSF13B2.64
22Multiple sclerosis 5EnrichmentTNFRSF1A2.64
23Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.64
24Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.64
25Immunodeficiency 53EnrichmentRELB2.64
26Bartsocas-papas syndrome 2EnrichmentCHUK2.64
27Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.64
28Immunodeficiency 112EnrichmentMAP3K142.64
29Common variable immunodeficiency phenotype due to homozygous taci deficiencyEnrichmentTNFRSF13B2.64
30Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.64
31Nik deficiencyEnrichmentMAP3K142.64
32Paget disease of bone 3EnrichmentSQSTM12.51
33Osteopetrosis, autosomal recessive 7EnrichmentTNFRSF11A2.51
34Immunodeficiency 16EnrichmentTNFRSF42.51
35Myopathy, distal, with rimmed vacuolesEnrichmentSQSTM12.51
36Frontotemporal dementia and/or amyotrophic lateral sclerosis 3EnrichmentSQSTM12.51
37Immunodeficiency with hyper-igm, type 1EnrichmentCD40LG2.51
38Immunodeficiency with hyper-igm, type 3EnrichmentCD402.51
39Cd40 ligand deficiencyEnrichmentCD40LG2.51
40Common variable immunodeficiency phenotype due to tweak deficiencyEnrichmentTNFSF122.51
41Immunodeficiency, common variable, 2EnrichmentTNFRSF13B2.34
42Immunodeficiency 33EnrichmentIKBKG2.34
43Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.34
44Immunodeficiency with hyper-igm, type 2EnrichmentTNFRSF13B2.34
45Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.34
46Immunodeficiency, common variable, 10EnrichmentNFKB22.34
47Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.34
48Immunodeficiency 127EnrichmentTNF2.34
49Rela fusion-positive ependymomaEnrichmentRELA2.34
50Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.34
51Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.34
52Intermittent hydrarthrosisEnrichmentTNFRSF1A2.34
53Common variable immunodeficiency 12EnrichmentNFKB12.34
54Familial expansile osteolysisEnrichmentTNFRSF11A2.21
55Paget disease of bone 5, juvenile-onsetEnrichmentTNFRSF11A2.21
56Welander distal myopathyEnrichmentSQSTM12.21
57Osteopetrosis, autosomal recessive 2EnrichmentTNFSF112.21
58Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onsetEnrichmentSQSTM12.21
59Intravascular large b-cell lymphomaEnrichmentBCL22.21
60Paget's disease of boneEnrichmentSQSTM12.21
61Spastic paraplegia-paget disease of bone syndromeEnrichmentSQSTM12.21
62Mycosis fungoidesEnrichmentTNFRSF1B2.16
63Psoriatic arthritisEnrichmentTNF2.16
64Nasopharyngeal carcinomaEnrichmentNFKBIA2.16
65Migraine without auraEnrichmentTNF2.16
66Saczary syndromeEnrichmentTNFRSF1B2.16
67Lymphoproliferative syndrome 2EnrichmentXIAP2.04
68Cerebral malariaEnrichmentTNF2.04
69DysosteosclerosisEnrichmentTNFRSF11A2.03
70High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL22.03
71Adult-onset myasthenia gravisEnrichmentTNFRSF11A2.03
72Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC31.94
73Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.94
74Vascular dementiaEnrichmentTNF1.94
75Herpes simplex virus encephalitisEnrichmentTRAF31.94
76Autosomal recessive osteopetrosisEnrichmentTNFSF111.91
77Pediatric systemic lupus erythematosusEnrichmentIRAK11.91
78Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.87
79Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.87
80Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.81
81Follicular lymphomaEnrichmentBCL21.81
82Charge syndromeEnrichmentTNFRSF1A1.69
83Coronary heart disease 5EnrichmentIKBKG1.69
84Primary biliary cholangitisEnrichmentTNFSF151.69
85Neuropathy, hereditary sensory and autonomic, type vEnrichmentNGF1.67
86Ciliary dyskinesia, primary, 3EnrichmentNFKB11.65
87Narcolepsy 1EnrichmentTNFSF41.61
88Immune deficiency diseaseEnrichmentRIPK11.60
89AsthmaEnrichmentTNF1.60
90Behavioral variant of frontotemporal dementiaEnrichmentSQSTM11.56
91Alzheimer's diseaseEnrichmentTNF1.53
92Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentSQSTM11.52
93Multiple sclerosisEnrichmentTNFRSF1A1.50
94GliosarcomaEnrichmentNFKBIA1.44
95Giant cell glioblastomaEnrichmentNFKBIA1.42
96Chromosome 1p36 deletion syndromeEnrichmentPRKCZ1.40
97Behcet syndromeEnrichmentTNFRSF1A1.37
98Multisystem inflammatory syndrome in childrenEnrichmentTRAF31.31
99Myocardial infarctionEnrichmentTNFSF41.18
100Severe combined immunodeficiencyEnrichmentIKBKB1.14
101Peripheral nervous system diseaseEnrichmentNGF1.02
102NeuropathyEnrichmentNGF1.02
103Hereditary breast ovarian cancer syndromeEnrichmentRIPK10.93
104Myeloma, multipleEnrichmentTRAF50.92
105Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentSQSTM10.78

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