IL12 signaling mediated by STAT4

No Pathway Network information available for IL12 signaling mediated by STAT4

Pathways in the IL12 signaling mediated by STAT4 SuperPath

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

Disorders associated with IL12 signaling mediated by STAT4 SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD247, CD3D, CD3E8.15
2Oligoarticular juvenile idiopathic arthritisEnrichmentCD247, IL2RA, STAT46.61
3Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD247, IL2RA, STAT46.61
4Severe combined immunodeficiencyEnrichmentCD247, CD3D, CD3E, CD3G6.31
5Idiopathic aplastic anemiaEnrichmentIFNG, PRF14.42
6Aplastic anemiaEnrichmentIFNG, PRF13.77
7Diffuse large b-cell lymphomaEnrichmentCREBBP, STAT33.19
8Type 1 diabetes mellitus 10EnrichmentIL2RA2.70
9Hemophagocytic lymphohistiocytosis, familial, 2EnrichmentPRF12.70
10Immunodeficiency 69EnrichmentIFNG2.70
11Disabling pansclerotic morphea of childhoodEnrichmentSTAT42.70
12Okt4 epitope deficiencyEnrichmentCD42.70
13T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.70
14Immunodeficiency 18EnrichmentCD3E2.70
15Systemic lupus erythematosus 11EnrichmentSTAT42.70
16Allergic rhinitisEnrichmentIL132.70
17Immunodeficiency 25EnrichmentCD2472.70
18Graham little-piccardi-lassueur syndromeEnrichmentHLA-DRA2.70
19Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.70
20Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.70
21Menke-hennekam syndrome 1EnrichmentCREBBP2.70
22Immunodeficiency 79EnrichmentCD42.70
23Immunodeficiency 88EnrichmentTBX212.70
24Immunodeficiency 19, severe combinedEnrichmentCD3D2.70
25Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.70
26Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.70
27Immunodeficiency 19EnrichmentCD3D2.70
28Menke-hennekam syndromeEnrichmentCREBBP2.70
29Fatal post-viral neurodegenerative disorderEnrichmentPRF12.70
30Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.70
31Camurati-engelmann disease 1EnrichmentTGFB12.40
32Thumb deformityEnrichmentCREBBP2.40
33Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA2.40
34Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.40
35Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.40
36Camurati-engelmann diseaseEnrichmentTGFB12.40
37Immunodeficiency 17EnrichmentCD3G2.40
38Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.40
39Immunodeficiency 117EnrichmentIRF12.40
40Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.22
41Asthma, nasal polyps, and aspirin intoleranceEnrichmentTBX212.22
42Mycosis fungoidesEnrichmentCD282.22
43Tuberous sclerosis 1EnrichmentIFNG2.22
44Hepatitis c virusEnrichmentIFNG2.22
45Tuberous sclerosis 2EnrichmentIFNG2.22
46Tethered spinal cord syndromeEnrichmentCREBBP2.22
47Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT32.22
48Hyper ige syndromeEnrichmentSTAT32.22
49Intraocular pressure quantitative trait locusEnrichmentCREBBP2.22
50Saczary syndromeEnrichmentCD282.22
51Congenital generalized lipodystrophyEnrichmentFOS2.10
52Pediatric systemic lupus erythematosusEnrichmentSTAT42.10
53Breast cancerEnrichmentIL2, JUN2.01
54Hemophagocytic lymphohistiocytosis, familial, 1EnrichmentPRF12.00
55Histiocytoid hemangiomaEnrichmentFOS2.00
56Rubinstein-taybi syndrome 1EnrichmentCREBBP1.92
57Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP1.92
58Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB11.92
59Il10-related early-onset inflammatory bowel diseaseEnrichmentTGFB11.92
60HypertrichosisEnrichmentCREBBP1.92
61Lymphoma, non-hodgkin, familialEnrichmentPRF11.80
62Permanent neonatal diabetes mellitusEnrichmentSTAT31.80
63AsthmaEnrichmentIL131.66
64Lung non-small cell carcinomaEnrichmentIRF11.66
65Acute promyelocytic leukemiaEnrichmentSTAT31.59
66Heart diseaseEnrichmentCREBBP1.56
67Corpus callosum, agenesis ofEnrichmentCREBBP1.53
68Isolated corpus callosum agenesisEnrichmentCREBBP1.53
69Rare genetic intellectual disabilityEnrichmentCREBBP1.53
70Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.53
71Human immunodeficiency virus type 1EnrichmentIFNG1.45
72Behcet syndromeEnrichmentSTAT41.43
73Cardiomyopathy, dilated, 1aEnrichmentNFATC21.39
74Autoinflammatory diseaseEnrichmentPRF11.33
75ScoliosisEnrichmentCREBBP1.33
76Lung cancerEnrichmentIRF11.21
77Cystic fibrosisEnrichmentTGFB11.21
78Systemic lupus erythematosusEnrichmentSTAT41.13
79Gastric cancerEnrichmentIRF11.08
80Myeloma, multipleEnrichmentCREBBP0.98
81AutismEnrichmentCREBBP0.87
82Congenital nervous system abnormalityEnrichmentCREBBP0.72
83Nervous system diseaseEnrichmentCREBBP0.72

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