Transcription_NF-kB signaling pathway

No Pathway Network information available for Transcription_NF-kB signaling pathway

Pathways in the Transcription_NF-kB signaling pathway SuperPath

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

Disorders associated with Transcription_NF-kB signaling pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA4.81
2Mycosis fungoidesEnrichmentCD28, TNFRSF1B4.33
3Psoriatic arthritisEnrichmentLTA, TNF4.33
4Immunodeficiency 7EnrichmentTRA, TRAC4.33
5Saczary syndromeEnrichmentCD28, TNFRSF1B4.33
6Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.49
7Behcet syndromeEnrichmentTLR4, TNFRSF1A2.59
8MalariaEnrichmentIKBKG, TNF2.43
9Precursor t-cell acute lymphoblastic leukemiaEnrichmentTRA, TRB2.43
10Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.40
11Proteus syndromeEnrichmentAKT12.40
12Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.40
13Neuropathy, hereditary sensory and autonomic, type iiiEnrichmentELP12.40
14Incontinentia pigmentiEnrichmentIKBKG2.40
15Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.40
16Immunodeficiency 68EnrichmentMYD882.40
17Leprosy 4EnrichmentLTA2.40
18Macroglobulinemia, waldenstrom 1EnrichmentMYD882.40
19Fetal encasement syndromeEnrichmentCHUK2.40
2046,xy sex reversal 6EnrichmentMAP3K12.40
21Immunodeficiency 15bEnrichmentIKBKB2.40
22Immunodeficiency 15aEnrichmentIKBKB2.40
23Immunodeficiency 92EnrichmentREL2.40
24Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.40
25Orofacial cleft 10EnrichmentSUMO12.40
26Chronic recurrent multifocal osteomyelitis 3EnrichmentIL1R12.40
27Asthma-related traits 5EnrichmentIRAK32.40
28Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.40
29Multiple sclerosis 5EnrichmentTNFRSF1A2.40
30Cowden syndrome 6EnrichmentAKT12.40
31Macular degeneration, age-related, 10EnrichmentTLR42.40
32Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.40
33Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.40
34Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.40
35Immunodeficiency 53EnrichmentRELB2.40
36Bartsocas-papas syndrome 2EnrichmentCHUK2.40
37Capillary hemangiomaEnrichmentAKT32.40
38Immunodeficiency 112EnrichmentMAP3K142.40
39Waldenstram macroglobulinemiaEnrichmentMYD882.40
40Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.40
41Nik deficiencyEnrichmentMAP3K142.40
42Akt2-related familial partial lipodystrophyEnrichmentAKT22.40
43Immunodeficiency 33EnrichmentIKBKG2.10
44Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.10
45Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.10
46Immunodeficiency, common variable, 10EnrichmentNFKB22.10
47Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.10
48Immunodeficiency 127EnrichmentTNF2.10
49Rela fusion-positive ependymomaEnrichmentRELA2.10
50Senior-loken syndrome 7EnrichmentAKT32.10
51Trypsinogen deficiencyEnrichmentTRB2.10
52Bardet-biedl syndrome 16EnrichmentAKT32.10
53Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.10
54Intermittent hydrarthrosisEnrichmentTNFRSF1A2.10
55Transient predisposition to invasive pyogenic bacterial infectionEnrichmentMYD882.10
56Common variable immunodeficiency 12EnrichmentNFKB12.10
57Submucosal cleft palateEnrichmentUBB2.10
58Cleft hard palateEnrichmentUBB2.10
59Systemic lupus erythematosusEnrichmentIRAK1, TNF1.98
60Uvula, bifidEnrichmentUBB1.92
61Cleft soft palateEnrichmentUBB1.92
62Nasopharyngeal carcinomaEnrichmentNFKBIA1.92
63Migraine without auraEnrichmentTNF1.92
64Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT31.80
65Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT31.80
66Immunodeficiency, common variable, 1EnrichmentNFKB21.80
67Cerebral malariaEnrichmentTNF1.80
68Pediatric systemic lupus erythematosusEnrichmentIRAK11.80
69Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.70
70Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.70
71Vitamin d-dependent rickets, type 2aEnrichmentTRB1.70
72Fabry diseaseEnrichmentELP11.70
73Vascular dementiaEnrichmentTNF1.70
74HemimegalencephalyEnrichmentAKT31.70
75Breast adenocarcinomaEnrichmentAKT11.63
76MegacolonEnrichmentAKT31.56
77Charge syndromeEnrichmentTNFRSF1A1.45
78Inflammatory bowel disease 1EnrichmentPRKCQ1.45
79Coronary heart disease 5EnrichmentIKBKG1.45
80Cowden syndromeEnrichmentAKT11.45
81Ciliary dyskinesia, primary, 3EnrichmentNFKB11.41
82PolymicrogyriaEnrichmentAKT31.41
83AsthmaEnrichmentTNF1.37
8446,xy complete gonadal dysgenesisEnrichmentMAP3K11.37
85MeningiomaEnrichmentAKT11.33
86Alzheimer's diseaseEnrichmentTNF1.30
87Multiple sclerosisEnrichmentTNFRSF1A1.26
88MedulloblastomaEnrichmentELP11.26
89Hereditary chronic pancreatitisEnrichmentTRB1.26
9046,xy partial gonadal dysgenesisEnrichmentMAP3K11.26
91Ovarian cancerEnrichmentAKT1, MAP3K11.21
92GliosarcomaEnrichmentNFKBIA1.21
93Pancreatitis, hereditaryEnrichmentTRB1.18
94Giant cell glioblastomaEnrichmentNFKBIA1.18
95Diffuse large b-cell lymphomaEnrichmentMYD881.14
96Myocardial infarctionEnrichmentLTA1.08
97Tooth agenesisEnrichmentSUMO11.08
98Multisystem inflammatory syndrome in childrenEnrichmentIRAK31.08
99Autoinflammatory diseaseEnrichmentTNFRSF1A1.04
100Severe combined immunodeficiencyEnrichmentIKBKB0.91
101Type 2 diabetes mellitusEnrichmentAKT20.81
102Hereditary breast carcinomaEnrichmentAKT10.79
103Breast cancerEnrichmentAKT10.59
104Colorectal cancerEnrichmentAKT10.53

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