Interleukin-12 family signaling

Pathway network for the Interleukin-12 family signaling SuperPath

Sources:
  • Reactome

Pathways in the Interleukin-12 family signaling SuperPath

Gene overlap in member pathways for Interleukin-12 family signaling SuperPath

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

Disorders associated with Interleukin-12 family signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK2, STAT39.39
2Behcet syndromeEnrichmentIL10, IL12A, IL23R, STAT45.98
3Primary biliary cholangitisEnrichmentIL12A, IL12RB13.38
4Cole-carpenter syndrome 1EnrichmentP4HB3.18
5Immunodeficiency 35EnrichmentTYK23.18
6Immunodeficiency 30EnrichmentIL12RB13.18
7Disabling pansclerotic morphea of childhoodEnrichmentSTAT43.18
8T-cell large granular lymphocyte leukemiaEnrichmentSTAT33.18
9Systemic lupus erythematosus 11EnrichmentSTAT43.18
10Psoriasis 7EnrichmentIL23R3.18
11Immunodeficiency 29EnrichmentIL12B3.18
12Inflammatory bowel disease 17EnrichmentIL23R3.18
13Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT33.18
14Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT33.18
15Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT33.18
16Stuve-wiedemann syndrome 2EnrichmentIL6ST3.09
17Hyper-ige syndrome 4a, autosomal dominant, with recurrent infectionsEnrichmentIL6ST3.09
18Immunodeficiency 31aEnrichmentSTAT13.09
19Immunodeficiency 31bEnrichmentSTAT13.09
20Hyper-ige syndrome 4b, autosomal recessive, with recurrent infectionsEnrichmentIL6ST3.09
21Immunodeficiency 94 with autoinflammation and dysmorphic faciesEnrichmentIL6ST3.09
22Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK13.09
23Human immunodeficiency virus type 1EnrichmentIFNG, IL102.94
24Thrombocythemia 3EnrichmentJAK22.88
25PolycythemiaEnrichmentJAK22.88
26Lymphomatoid papulosisEnrichmentTYK22.88
27Hypereosinophilic syndromeEnrichmentJAK22.88
28Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK22.88
29Immunodeficiency 31cEnrichmentSTAT12.79
30Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.79
31Cold-induced sweating syndrome including crisponi syndromeEnrichmentCRLF12.79
32Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.70
33Takayasu arteritisEnrichmentIL12B2.70
34Polycythemia veraEnrichmentJAK22.70
35Hyper ige syndromeEnrichmentSTAT32.70
36Cole-carpenter syndromeEnrichmentP4HB2.70
37Stuve-wiedemann syndrome 1EnrichmentIL6ST2.61
38Cone-rod dystrophy 12EnrichmentCRLF12.61
39Cold-induced sweating syndromeEnrichmentCRLF12.61
40Stüve-wiedemann syndromeEnrichmentIL6ST2.61
41Erythrocytosis, familial, 1EnrichmentJAK22.58
42Budd-chiari syndromeEnrichmentJAK22.58
43Pediatric systemic lupus erythematosusEnrichmentSTAT42.58
44Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typicalEnrichmentLMNB12.55
45Immunodeficiency 50EnrichmentMSN2.55
46Muscular dystrophy, limb-girdle, autosomal dominant 3EnrichmentHNRNPDL2.55
47Microvascular complications of diabetes 6EnrichmentSOD22.55
48Even-plus syndromeEnrichmentHSPA92.55
49Anemia, sideroblastic, 4EnrichmentHSPA92.55
50Hiatt-neu-cooper neurodevelopmental syndromeEnrichmentRALA2.55
51Immunodeficiency 69EnrichmentIFNG2.55
52Knobloch syndrome 2EnrichmentPAK22.55
53Intellectual developmental disorder with polymicrogyria and seizuresEnrichmentTCP12.55
54Graft-versus-host diseaseEnrichmentIL102.55
55Adult onset demyelinating leukodystrophyEnrichmentLMNB12.55
56Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic faciesEnrichmentRAP1B2.55
57Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2EnrichmentHNRNPA2B12.55
58Microcephaly 26, primary, autosomal dominantEnrichmentLMNB12.55
59Takenouchi-kosaki syndromeEnrichmentCDC422.55
60Oculopharyngeal muscular dystrophy 2EnrichmentHNRNPA2B12.55
61Nocarh syndromeEnrichmentCDC422.55
62Cold-induced sweating syndrome 1EnrichmentCRLF12.49
63Idiopathic achalasiaEnrichmentCRLF12.49
64Myeloproliferative neoplasmEnrichmentJAK22.48
65Osteogenesis imperfecta, type iEnrichmentP4HB2.40
66Crisponi/cold-induced sweating syndrome 1EnrichmentCRLF12.39
67MyelofibrosisEnrichmentJAK22.33
68Essential thrombocythemiaEnrichmentJAK22.33
69Oligoarticular juvenile idiopathic arthritisEnrichmentSTAT42.33
70Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentSTAT42.33
71Chronic mucocutaneous candidiasisEnrichmentSTAT12.31
72Permanent neonatal diabetes mellitusEnrichmentSTAT32.28
73Systemic lupus erythematosusEnrichmentIL10, STAT42.28
74Diaphyseal medullary stenosis with malignant fibrous histiocytomaEnrichmentMTAP2.25
75Periventricular nodular heterotopia 8EnrichmentARF12.25
76Transaldolase deficiencyEnrichmentTALDO12.25
77Spastic tetraplegia and axial hypotonia, progressiveEnrichmentSOD12.25
78Immune system diseaseEnrichmentCDC422.25
79Autosomal dominant primary microcephalyEnrichmentLMNB12.25
80AcromegalyEnrichmentAIP2.25
81Autosomal recessive sideroblastic anemiaEnrichmentHSPA92.25
82Null pituitary adenomaEnrichmentAIP2.25
83Diaphyseal medullary stenosis-bone malignancy syndromeEnrichmentMTAP2.25
84Familial isolated pituitary adenomaEnrichmentAIP2.25
85Silent pituitary adenomaEnrichmentAIP2.25
86GigantismEnrichmentAIP2.25
87Leukemia, acute lymphoblastic 3EnrichmentJAK22.22
88Tuberous sclerosis 1EnrichmentIFNG2.08
89Hepatitis c virusEnrichmentIFNG2.08
90Tuberous sclerosis 2EnrichmentIFNG2.08
91Pituitary adenoma 1, multiple typesEnrichmentAIP2.08
92Inclusion body myopathy with paget disease of bone and frontotemporal dementiaEnrichmentHNRNPA2B12.08
93Growth hormone secreting pituitary adenomaEnrichmentAIP2.08
94Aip familial isolated pituitary adenomasEnrichmentAIP2.08
95Acute promyelocytic leukemiaEnrichmentSTAT32.07
96Myopathy, autophagic vacuolar, infantile-onsetEnrichmentHNRNPA2B11.95
97Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC421.95
98ProlactinomaEnrichmentAIP1.95
99Knobloch syndromeEnrichmentPAK21.95
100Systemic-onset juvenile idiopathic arthritisEnrichmentMIF1.95
101Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentHNRNPA2B1, SOD11.94
102Diffuse large b-cell lymphomaEnrichmentSTAT31.90
103Rheumatoid arthritis, systemic juvenileEnrichmentMIF1.86
104Knobloch syndrome 1EnrichmentPAK21.86
105Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentSOD11.86
106Idiopathic aplastic anemiaEnrichmentIFNG1.86
107Il10-related early-onset inflammatory bowel diseaseEnrichmentIL101.78
108Motor neuron diseaseEnrichmentSOD11.71
109Rheumatoid arthritisEnrichmentIL101.60
110Leukemia, acute myeloidEnrichmentJAK21.58
111Amyotrophic lateral sclerosis 1EnrichmentSOD11.56
112Aplastic anemiaEnrichmentIFNG1.56
113Primary ovarian insufficiencyEnrichmentJAK21.41
114Periventricular nodular heterotopiaEnrichmentARF11.41
11546,xy partial gonadal dysgenesisEnrichmentVAMP71.32
116Cystic fibrosisEnrichmentMIF1.07
117Hereditary breast ovarian cancer syndromeEnrichmentLCP10.84
118Complex neurodevelopmental disorderEnrichmentRALA0.53
119Inherited cancer-predisposing syndromeEnrichmentAIP0.51

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