Development_Thrombopoetin signaling via JAK-STAT pathway

No Pathway Network information available for Development_Thrombopoetin signaling via JAK-STAT pathway

Pathways in the Development_Thrombopoetin signaling via JAK-STAT pathway SuperPath

#NameSourceGenes
1Development_Thrombopoetin signaling via JAK-STAT pathwayGeneGo (Thomson Reuters)

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

Disorders associated with Development_Thrombopoetin signaling via JAK-STAT pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Essential thrombocythemiaEnrichmentJAK2, MPL, THPO6.83
2Congenital amegakaryocytic thrombocytopeniaEnrichmentMPL, THPO5.56
3Dyskeratosis congenita, autosomal dominant 6EnrichmentMPL, THPO5.08
4Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK2, STAT35.08
5Multiple endocrine neoplasia, type iEnrichmentCDKN1A, CDKN1B4.24
6MyelofibrosisEnrichmentJAK2, MPL4.24
7ThrombocytopeniaEnrichmentMPL, PTPN11, THPO4.15
8Acute promyelocytic leukemiaEnrichmentSTAT3, STAT5B3.67
9Diffuse large b-cell lymphomaEnrichmentSOCS1, STAT33.34
10MetachondromatosisEnrichmentPTPN112.77
11Thrombocythemia 2EnrichmentMPL2.77
12Dermatitis, atopic, 4EnrichmentSOCS32.77
13Leopard syndrome 1EnrichmentPTPN112.77
14Amegakaryocytic thrombocytopenia, congenital, 1EnrichmentMPL2.77
15Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominantEnrichmentSTAT5B2.77
16Amegakaryocytic thrombocytopenia, congenital, 2EnrichmentTHPO2.77
17T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.77
18Neuroendocrine tumorEnrichmentCDKN1B2.77
19Immunodeficiency 31aEnrichmentSTAT12.77
20Hereditary thrombocytosis with transverse limb defectEnrichmentTHPO2.77
21Immunodeficiency 31bEnrichmentSTAT12.77
22Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.77
23Thrombocytopenia 9EnrichmentTHPO2.77
24Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.77
25Vegetative pyoderma gangrenosumEnrichmentPTPN62.77
26Bullous pyoderma gangrenosumEnrichmentPTPN62.77
27Pustular pyoderma gangrenosumEnrichmentPTPN62.77
28Classic pyoderma gangrenosumEnrichmentPTPN62.77
29Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.77
30Malignant astrocytomaEnrichmentPTPN112.77
31Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessiveEnrichmentSTAT5B2.47
32Thrombocythemia 3EnrichmentJAK22.47
33Multiple endocrine neoplasia, type ivEnrichmentCDKN1B2.47
34Immunodeficiency 31cEnrichmentSTAT12.47
35Werner syndromeEnrichmentPTPN112.47
36PolycythemiaEnrichmentJAK22.47
37Hypereosinophilic syndromeEnrichmentJAK22.47
38Laron syndrome with immunodeficiencyEnrichmentSTAT5B2.47
39Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.29
40Thrombocythemia 1EnrichmentTHPO2.29
41Immune thrombocytopeniaEnrichmentSOCS12.29
42Polycythemia veraEnrichmentJAK22.29
43Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.29
44Autoinflammatory syndrome, familial, with or without immunodeficiencyEnrichmentSOCS12.29
45Bacteremia 2EnrichmentCISH2.29
46Hyper ige syndromeEnrichmentSTAT32.29
47Tricuspid valve insufficiencyEnrichmentPTPN112.29
48Erythrocytosis, familial, 1EnrichmentJAK22.17
49Anemia, autoimmune hemolyticEnrichmentSOCS12.17
50Budd-chiari syndromeEnrichmentJAK22.17
51Mhc class i deficiency 1EnrichmentTAP12.17
52Mantle cell lymphomaEnrichmentCCND12.17
53Mhc class i deficiencyEnrichmentTAP12.17
54TuberculosisEnrichmentCISH2.17
55Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.17
56Noonan syndrome with multiple lentiginesEnrichmentPTPN112.17
57Immunodeficiency by defective expression of mhc class iEnrichmentTAP12.17
58Primary hyperparathyroidismEnrichmentCDKN1B2.17
59Von hippel-lindau syndromeEnrichmentCCND12.07
60LymphomaEnrichmentPTPN112.07
61Myeloproliferative neoplasmEnrichmentJAK22.07
62Patent ductus arteriosusEnrichmentPTPN111.99
63Chronic mucocutaneous candidiasisEnrichmentSTAT11.99
64Noonan syndrome 3EnrichmentPTPN111.93
65Permanent neonatal diabetes mellitusEnrichmentSTAT31.87
66Leukemia, acute lymphoblastic 3EnrichmentJAK21.82
67Leukemia, chronic lymphocyticEnrichmentCCND11.77
68Pectus excavatumEnrichmentPTPN111.73
69Specific learning disabilityEnrichmentPTPN111.73
70EpicanthusEnrichmentPTPN111.70
71Juvenile myelomonocytic leukemiaEnrichmentPTPN111.70
72Congenital long qt syndromeEnrichmentPTPN111.70
73Inherited cancer-predisposing syndromeEnrichmentCDKN1B, PTPN111.68
74Noonan syndrome and noonan-related syndromeEnrichmentPTPN111.60
75Patent foramen ovaleEnrichmentPTPN111.52
76Noonan syndrome 1EnrichmentPTPN111.42
77MalariaEnrichmentCISH1.42
78ScoliosisEnrichmentPTPN111.40
79Hydrops fetalis, nonimmuneEnrichmentPTPN111.36
80RasopathyEnrichmentPTPN111.36
81StrabismusEnrichmentPTPN111.35
82Bladder cancerEnrichmentCDKN1A1.32
83Long qt syndrome 1EnrichmentPTPN111.30
84Non-immune hydrops fetalisEnrichmentPTPN111.29
85NephronophthisisEnrichmentPIAS11.26
86Systemic lupus erythematosusEnrichmentSOCS11.19
87Leukemia, acute myeloidEnrichmentJAK21.18
88Hypertrophic cardiomyopathyEnrichmentPTPN111.15
89Myeloma, multipleEnrichmentCCND11.04
90Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.04
91Primary ovarian insufficiencyEnrichmentJAK21.02
92Colorectal cancerEnrichmentCCND10.86
93Ovarian cancerEnrichmentCDKN1B0.80
94Autism spectrum disorderEnrichmentPTPN110.77
95MicrocephalyEnrichmentPTPN110.72

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