Regulatory circuits of the STAT3 signaling pathway

No Pathway Network information available for Regulatory circuits of the STAT3 signaling pathway

Pathways in the Regulatory circuits of the STAT3 signaling pathway SuperPath

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

Disorders associated with Regulatory circuits of the STAT3 signaling pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Specific learning disabilityEnrichmentGHR, MAPK13.79
2Amyloidosis, primary localized cutaneous, 1EnrichmentOSMR2.75
3Thrombocythemia 2EnrichmentMPL2.75
4Dermatitis, atopic, 4EnrichmentSOCS32.75
5Amegakaryocytic thrombocytopenia, congenital, 1EnrichmentMPL2.75
6Noonan syndrome 13EnrichmentMAPK12.75
7Laron syndromeEnrichmentGHR2.75
8T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.75
9Growth hormone insensitivity, partialEnrichmentGHR2.75
10Interleukin 6, serum level of, quantitative trait locusEnrichmentIL6R2.75
11Soluble interleukin-6 receptor, serum level of, quantitative trait locusEnrichmentIL6R2.75
12Hyper-ige syndrome 5, autosomal recessive, with recurrent infectionsEnrichmentIL6R2.75
13Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.75
14Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.75
15Chronic neutrophilic leukemiaEnrichmentCSF3R2.75
16Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.75
17Neutrophilia, hereditaryEnrichmentCSF3R2.45
18Growth hormone deficiency, isolated partialEnrichmentGHR2.45
19Neutropenia, severe congenital, 7, autosomal recessiveEnrichmentCSF3R2.45
20Immunodeficiency 31cEnrichmentIL21R2.45
21Primary cutaneous amyloidosisEnrichmentOSMR2.45
22Immunodeficiency 56EnrichmentIL21R2.45
23Severe congenital neutropenia 7EnrichmentCSF3R2.45
24Congenital amegakaryocytic thrombocytopeniaEnrichmentMPL2.45
25Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.28
26Stuve-wiedemann syndrome 1EnrichmentLIFR2.28
27Dyskeratosis congenita, autosomal dominant 6EnrichmentMPL2.28
28Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR2.28
29Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT32.28
30Hyper ige syndromeEnrichmentSTAT32.28
31Neonatal inflammatory skin and bowel diseaseEnrichmentEGFR2.28
32Stüve-wiedemann syndromeEnrichmentLIFR2.28
33Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.15
34Cowden syndrome 1EnrichmentEGFR1.98
35Lung squamous cell carcinomaEnrichmentEGFR1.98
36MyelofibrosisEnrichmentMPL1.91
37Squamous cell carcinoma, head and neckEnrichmentEGFR1.91
38Essential thrombocythemiaEnrichmentMPL1.91
39Lennox-gastaut syndromeEnrichmentMAPK101.85
40Severe congenital neutropeniaEnrichmentCSF3R1.85
41Permanent neonatal diabetes mellitusEnrichmentSTAT31.85
42Atypical chronic myeloid leukemia, bcr-abl1 negativeEnrichmentCSF3R1.80
43Lung non-small cell carcinomaEnrichmentEGFR1.71
44Lip and oral cavity carcinomaEnrichmentEGFR1.68
45Hypercholesterolemia, familial, 1EnrichmentGHR1.64
46Acute promyelocytic leukemiaEnrichmentSTAT31.64
47Lung cancer susceptibility 3EnrichmentEGFR1.61
48Familial hypercholesterolemiaEnrichmentGHR1.58
49GliosarcomaEnrichmentEGFR1.55
50Giant cell glioblastomaEnrichmentEGFR1.53
51Heart, malformation ofEnrichmentMAPK11.50
52Arteriovenous malformations of the brainEnrichmentEGFR1.48
53Diffuse large b-cell lymphomaEnrichmentSTAT31.48
54Bladder cancerEnrichmentEGFR1.30
55Lung cancerEnrichmentEGFR1.26
56CakutEnrichmentLIFR1.23
57ThrombocytopeniaEnrichmentMPL1.09
58SchizophreniaEnrichmentPTPRT1.00
59AutismEnrichmentPTPRT0.92
60Ovarian cancerEnrichmentEGFR0.78
61MicrocephalyEnrichmentMAPK10.71
62Inherited cancer-predisposing syndromeEnrichmentEGFR0.68

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