Signaling by CSF3 (G-CSF)

No Pathway Network information available for Signaling by CSF3 (G-CSF)

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

Disorders associated with Signaling by CSF3 (G-CSF) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK2, STAT38.26
2Noonan syndrome 3EnrichmentKRAS, PTPN114.01
3Acute promyelocytic leukemiaEnrichmentSTAT3, STAT5B3.60
4Juvenile myelomonocytic leukemiaEnrichmentKRAS, PTPN113.51
5Noonan syndrome and noonan-related syndromeEnrichmentKRAS, PTPN113.31
6Diffuse large b-cell lymphomaEnrichmentSOCS1, STAT33.26
7Noonan syndrome 1EnrichmentKRAS, PTPN112.93
8RasopathyEnrichmentKRAS, PTPN112.83
9Immunodeficiency 35EnrichmentTYK22.73
10Dermatitis, atopic, 4EnrichmentSOCS32.73
11Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominantEnrichmentSTAT5B2.73
12Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.73
13T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.73
14Immunodeficiency 31aEnrichmentSTAT12.73
15Immunodeficiency 31bEnrichmentSTAT12.73
16Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.73
17Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.73
18Autoinflammation with pulmonary and cutaneous vasculitisEnrichmentHCK2.73
19ColitisEnrichmentSYK2.73
20Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.73
21Chronic neutrophilic leukemiaEnrichmentCSF3R2.73
22Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.73
23Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.73
24Non-immune hydrops fetalisEnrichmentKRAS, PTPN112.68
25MetachondromatosisEnrichmentPTPN112.66
26Oculoectodermal syndromeEnrichmentKRAS2.66
27Leopard syndrome 1EnrichmentPTPN112.66
28Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.66
29Congenital pulmonary airway malformationEnrichmentKRAS2.66
30Malignant astrocytomaEnrichmentPTPN112.66
31Leukemia, acute myeloidEnrichmentJAK2, KRAS2.46
32Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessiveEnrichmentSTAT5B2.43
33Neutrophilia, hereditaryEnrichmentCSF3R2.43
34Thrombocythemia 3EnrichmentJAK22.43
35Neutropenia, severe congenital, 7, autosomal recessiveEnrichmentCSF3R2.43
36Immunodeficiency 31cEnrichmentSTAT12.43
37Severe congenital neutropenia 7EnrichmentCSF3R2.43
38Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.43
39PolycythemiaEnrichmentJAK22.43
40Lymphomatoid papulosisEnrichmentTYK22.43
41ArthritisEnrichmentSYK2.43
42Hypereosinophilic syndromeEnrichmentJAK22.43
43Laron syndrome with immunodeficiencyEnrichmentSTAT5B2.43
44Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK22.43
45Submucosal cleft palateEnrichmentUBB2.43
46Cleft hard palateEnrichmentUBB2.43
47Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.35
48Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS2.35
49Werner syndromeEnrichmentPTPN112.35
50Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.26
51Immune thrombocytopeniaEnrichmentSOCS12.26
52Polycythemia veraEnrichmentJAK22.26
53Uvula, bifidEnrichmentUBB2.26
54Cleft soft palateEnrichmentUBB2.26
55Autoinflammatory syndrome, familial, with or without immunodeficiencyEnrichmentSOCS12.26
56Hyper ige syndromeEnrichmentSTAT32.26
57Tricuspid valve insufficiencyEnrichmentPTPN112.18
58Erythrocytosis, familial, 1EnrichmentJAK22.13
59Anemia, autoimmune hemolyticEnrichmentSOCS12.13
60Budd-chiari syndromeEnrichmentJAK22.13
61Schimmelpenning-feuerstein-mims syndromeEnrichmentKRAS2.05
62Cardiofaciocutaneous syndrome 1EnrichmentKRAS2.05
63Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS2.05
64Cardiofaciocutaneous syndromeEnrichmentKRAS2.05
65Lung sarcomatoid carcinomaEnrichmentKRAS2.05
66Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS2.05
67Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.05
68Noonan syndrome with multiple lentiginesEnrichmentPTPN112.05
69Pilocytic astrocytomaEnrichmentKRAS2.05
70Myeloproliferative neoplasmEnrichmentJAK22.04
71Chronic mucocutaneous candidiasisEnrichmentSTAT11.96
72LymphomaEnrichmentPTPN111.96
73Breast cancerEnrichmentKRAS, SHC11.93
74MyelofibrosisEnrichmentJAK21.89
75Essential thrombocythemiaEnrichmentJAK21.89
76Patent ductus arteriosusEnrichmentPTPN111.88
77Breast adenocarcinomaEnrichmentKRAS1.88
78Lung squamous cell carcinomaEnrichmentKRAS1.88
79Severe congenital neutropeniaEnrichmentCSF3R1.83
80Permanent neonatal diabetes mellitusEnrichmentSTAT31.83
81Nevus, epidermalEnrichmentKRAS1.81
82Capillary malformation-arteriovenous malformation 1EnrichmentKRAS1.81
83Leukemia, chronic myeloidEnrichmentKRAS1.81
84Gallbladder cancerEnrichmentKRAS1.81
85Pilomyxoid astrocytomaEnrichmentKRAS1.81
86Leukemia, acute lymphoblastic 3EnrichmentJAK21.78
87Atypical chronic myeloid leukemia, bcr-abl1 negativeEnrichmentCSF3R1.78
88Immune deficiency diseaseEnrichmentSYK1.70
89Pectus excavatumEnrichmentPTPN111.62
90Lung non-small cell carcinomaEnrichmentKRAS1.62
91Specific learning disabilityEnrichmentPTPN111.62
92EpicanthusEnrichmentPTPN111.58
93Congenital long qt syndromeEnrichmentPTPN111.58
94Lung cancer susceptibility 3EnrichmentKRAS1.52
95Lynch syndromeEnrichmentKRAS1.49
96Patent foramen ovaleEnrichmentPTPN111.41
97Arteriovenous malformations of the brainEnrichmentKRAS1.38
98ScoliosisEnrichmentPTPN111.29
99Pancreatic cancerEnrichmentKRAS1.27
100Hydrops fetalis, nonimmuneEnrichmentPTPN111.25
101StrabismusEnrichmentPTPN111.24
102Bladder cancerEnrichmentKRAS1.21
103Differentiated thyroid carcinomaEnrichmentKRAS1.21
104Long qt syndrome 1EnrichmentPTPN111.19
105Lung cancerEnrichmentKRAS1.16
106Systemic lupus erythematosusEnrichmentSOCS11.16
107Gastric cancerEnrichmentKRAS1.04
108Hypertrophic cardiomyopathyEnrichmentPTPN111.04
109Hereditary breast carcinomaEnrichmentKRAS1.03
110ThrombocytopeniaEnrichmentPTPN111.00
111Primary ovarian insufficiencyEnrichmentJAK20.99
112Hereditary breast ovarian cancer syndromeEnrichmentKRAS0.94
113Myeloma, multipleEnrichmentKRAS0.93
114Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.93
115Ovarian cancerEnrichmentKRAS0.70
116Autism spectrum disorderEnrichmentPTPN110.67
117MicrocephalyEnrichmentPTPN110.62
118Inherited cancer-predisposing syndromeEnrichmentPTPN110.59

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