CLEC7A (Dectin-1) signaling

Pathway network for the CLEC7A (Dectin-1) signaling SuperPath

Sources:
  • Reactome
  • PubChem

Pathways in the CLEC7A (Dectin-1) signaling SuperPath

#NameSourceGenes
1CLEC7A (Dectin-1) signalingReactome
2C-type lectin receptors (CLRs)Reactome
3Fc epsilon receptor (FCERI) signalingReactome
4Role of LAT2/NTAL/LAB on calcium mobilizationReactome
5Alternative NF-kappaB pathwayPubChem

Gene overlap in member pathways for CLEC7A (Dectin-1) signaling SuperPath

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

Disorders associated with CLEC7A (Dectin-1) signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Nevus, epidermalEnrichmentHRAS, KRAS, NRAS, PIK3CA6.80
2Lung non-small cell carcinomaEnrichmentHRAS, KRAS, NRAS, PIK3CA5.84
3Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS5.65
4Common variable immunodeficiencyEnrichmentNFKB1, NFKB25.47
5Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.47
6Noonan syndrome and noonan-related syndromeEnrichmentHRAS, KRAS, NRAS, SOS15.24
7Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R25.16
8Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM1, CALM2, CALM34.90
9Noonan syndrome 3EnrichmentHRAS, KRAS, SOS14.72
10Long qt syndrome 1EnrichmentCALM1, CALM2, CALM3, ITPR34.48
11Noonan syndrome 1EnrichmentHRAS, KRAS, NRAS, SOS14.45
12Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA4.42
13Melanocytic nevus syndrome, congenitalEnrichmentHRAS, NRAS, RAF14.37
14RasopathyEnrichmentHRAS, KRAS, NRAS, SOS14.23
15Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS4.16
16Large congenital melanocytic nevusEnrichmentHRAS, NRAS3.69
17Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS3.39
18Fetal encasement syndromeEnrichmentCHUK3.35
19Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB23.35
20Immunodeficiency 53EnrichmentRELB3.35
21Bartsocas-papas syndrome 2EnrichmentCHUK3.35
22Immunodeficiency 112EnrichmentMAP3K143.35
23Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK3.35
24Nik deficiencyEnrichmentMAP3K143.35
25Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB13.05
26Immunodeficiency, common variable, 10EnrichmentNFKB23.05
27Common variable immunodeficiency 12EnrichmentNFKB13.05
28Breast adenocarcinomaEnrichmentKRAS, PIK3CA3.00
29Lung squamous cell carcinomaEnrichmentKRAS, PIK3CA3.00
30Isolated split hand-split foot malformationEnrichmentBTRC, SEM12.98
31MacrodactylyEnrichmentPIK3CA2.96
32Noonan syndrome 4EnrichmentSOS12.96
33Megalencephaly, autosomal dominantEnrichmentPIK3CA2.96
34Cowden syndrome 5EnrichmentPIK3CA2.96
35Cerebral cavernous malformations 4EnrichmentPIK3CA2.96
36Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.96
37Short syndromeEnrichmentPIK3R12.96
38Hemifacial myohyperplasiaEnrichmentPIK3CA2.96
39Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.96
40Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.96
41Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.96
42Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.96
43Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.96
44HypospadiasEnrichmentPIK3CA2.96
45ColitisEnrichmentSYK2.96
46Rare venous malformationEnrichmentPIK3CA2.96
47Diaphragmatic eventrationEnrichmentPIK3CA2.96
48Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.96
49Rare combined vascular malformationEnrichmentPIK3CA2.96
50Cavernous lymphangiomaEnrichmentPIK3CA2.96
51Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.96
52Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.96
53Eccrine angiomatous hamartomaEnrichmentPIK3CA2.96
54Macrodactyly of toeEnrichmentPIK3CA2.96
55Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3002.90
56Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3002.90
57Thyroid cancer, nonmedullary, 2EnrichmentHRAS, NRAS2.85
58Capillary malformation-arteriovenous malformation 1EnrichmentKRAS, PIK3CA2.85
59Leukemia, chronic myeloidEnrichmentKRAS, NRAS2.85
60Gallbladder cancerEnrichmentKRAS, PIK3CA2.85
61Follicular thyroid carcinomaEnrichmentHRAS, NRAS2.85
62Pilomyxoid astrocytomaEnrichmentKRAS, RAF12.76
63Bladder cancerEnrichmentHRAS, KRAS, PIK3CA2.76
64Differentiated thyroid carcinomaEnrichmentHRAS, KRAS, NRAS2.76
65Immunodeficiency, common variable, 1EnrichmentNFKB22.75
66Fibromatosis, gingival, 1EnrichmentSOS12.66
67Pulmonic stenosisEnrichmentSOS12.66
68Keratosis, seborrheicEnrichmentPIK3CA2.66
69Noonan syndrome 8EnrichmentPIK3CA2.66
70Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.66
71ArthritisEnrichmentSYK2.66
72Arteriovenous malformationEnrichmentHRAS, PIK3CA2.62
73Ellis-van creveld syndromeEnrichmentPRKACA, PRKACB2.53
74Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, PIK3CA2.53
75Breast cancerEnrichmentPIK3CA, SHC12.52
76Pompe disease, infantile-onsetEnrichmentPIK3CA2.48
77Nuchal bleb, familialEnrichmentSOS12.48
78Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.48
79Immunodeficiency 14EnrichmentPIK3R12.48
80KeratoacanthomaEnrichmentPIK3CA2.48
81Colorectal cancerEnrichmentPIK3CA, PIK3R12.39
82Juvenile myelomonocytic leukemiaEnrichmentKRAS, NRAS2.37
83Lip and oral cavity carcinomaEnrichmentHRAS, PIK3CA2.37
84Ciliary dyskinesia, primary, 3EnrichmentNFKB12.35
85Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R22.35
86Cerebrovascular diseaseEnrichmentPIK3CA2.35
87Familial cerebral cavernous malformationsEnrichmentPIK3CA2.35
88Gingival fibromatosisEnrichmentSOS12.35
89Aortic valve disease 1EnrichmentSOS1, TAB22.30
90Patent foramen ovaleEnrichmentPSMC3, TAB22.26
91Capillary malformations, congenitalEnrichmentPIK3CA2.26
92HemimegalencephalyEnrichmentPIK3CA2.26
9346,xy partial gonadal dysgenesisEnrichmentMAP3K1, SOS12.23
94Anhidrosis, isolated, with normal sweat glandsEnrichmentITPR22.21
95Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.21
96Immunodeficiency 103 fungal infectionsEnrichmentCARD92.21
97Incontinentia pigmentiEnrichmentIKBKG2.21
98Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.21
99Caspase 8 deficiencyEnrichmentCASP82.21
100Frontometaphyseal dysplasia 2EnrichmentMAP3K72.21
101Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.21
102Immunodeficiency 15bEnrichmentIKBKB2.21
103Neurodevelopmental disorder with microcephaly, hypotonia, and absent languageEnrichmentPSMB12.21
104Immunodeficiency 15aEnrichmentIKBKB2.21
105Charcot-marie-tooth disease, demyelinating, type 1jEnrichmentITPR32.21
106Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.21
107Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.21
108Neurodevelopmental, jaw, eye, and digital syndromeEnrichmentFBXW112.21
109Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.21
110Stankiewicz-isidor syndromeEnrichmentPSMD122.21
111Candidiasis, familial, 4EnrichmentCLEC7A2.21
112Deafness, cataract, impaired intellectual development, and polyneuropathyEnrichmentPSMC32.21
113Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.21
114Long qt syndrome 16EnrichmentCALM32.21
115Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.21
116Thrombocytopenia 6EnrichmentSRC2.21
117Long qt syndrome 15EnrichmentCALM22.21
118Immunodeficiency 133 with ectodermal dysplasia with or without peripheral neuropathyEnrichmentITPR32.21
119Polyvalvular heart disease syndromeEnrichmentTAB22.21
120Klippel-trenaunay-weber syndromeEnrichmentPIK3CA2.18
121Cowden syndrome 1EnrichmentPIK3CA2.18
122Hemihyperplasia, isolatedEnrichmentPIK3CA2.18
123Lynch syndromeEnrichmentKRAS, PIK3CA2.17
124Overgrowth syndromeEnrichmentPIK3R12.11
125Rare genetic intellectual disabilityEnrichmentCREBBP, EP3002.08
126Oculoectodermal syndromeEnrichmentKRAS2.08
127Melanosis, neurocutaneousEnrichmentNRAS2.08
128Bleeding disorder, platelet-type, 18EnrichmentRASGRP22.08
129Noonan syndrome 6EnrichmentNRAS2.08
13046,xy sex reversal 6EnrichmentMAP3K12.08
131Immunodeficiency 64 with lymphoproliferationEnrichmentRASGRP12.08
132Noonan syndrome 13EnrichmentMAPK12.08
133Immunodeficiency 81EnrichmentLCP22.08
134Knobloch syndrome 2EnrichmentPAK22.08
135Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.08
136Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.08
137Isolated growth hormone deficiency type iiiEnrichmentBTK2.08
138Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.08
139Lymphoproliferative syndrome 1EnrichmentITK2.08
140Congenital pulmonary airway malformationEnrichmentKRAS2.08
141Immunodeficiency 64EnrichmentRASGRP12.08
142Ebv-induced lymphoproliferative disease due to rasgrp1 deficiencyEnrichmentRASGRP12.08
143Phakomatosis pigmentokeratoticaEnrichmentHRAS2.08
144Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.08
145Neurocutaneous melanocytosisEnrichmentNRAS2.08
146Intellectual developmental disorder, x-linked 30EnrichmentPAK32.03
147Noonan syndrome 5EnrichmentRAF12.03
148Tubulointerstitial kidney disease, autosomal dominant 2EnrichmentMUC12.03
149Cardiomyopathy, dilated, 1nnEnrichmentRAF12.03
150Cardioacrofacial dysplasia 2EnrichmentPRKACB2.03
151Leopard syndrome 2EnrichmentRAF12.03
152Dengue virusEnrichmentCD2092.03
153Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.03
154Cardioacrofacial dysplasia 1EnrichmentPRKACA2.03
155Menke-hennekam syndrome 1EnrichmentCREBBP2.03
156TrigonitisEnrichmentRAF12.03
157Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.03
158Menke-hennekam syndromeEnrichmentCREBBP2.03
159Extrinsic allergic alveolitisEnrichmentMUC5B2.03
160Adult hepatocellular carcinomaEnrichmentPIK3CA2.00
161Cowden syndromeEnrichmentPIK3CA2.00
162Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.96
163Immune deficiency diseaseEnrichmentSYK1.92
164Spinocerebellar ataxia 29EnrichmentITPR11.91
165Immunodeficiency 33EnrichmentIKBKG1.91
166Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA1.91
167Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM11.91
168AspergillosisEnrichmentCLEC7A1.91
169Long qt syndrome 14EnrichmentCALM11.91
170Birk-aharoni syndromeEnrichmentPSMC11.91
171Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA1.91
172Proteasome-associated autoinflammatory syndrome 3EnrichmentPSMB41.91
173Rela fusion-positive ependymomaEnrichmentRELA1.91
174Congenital heart defects, multiple types, 2EnrichmentTAB21.91
175Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG1.91
17617q24.2 microdeletion syndromeEnrichmentPSMD121.91
177Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC21.91
178Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB21.91
179Submucosal cleft palateEnrichmentUBB1.91
180Cleft hard palateEnrichmentUBB1.91
181MeningiomaEnrichmentPIK3CA1.88
182Nk-cell enteropathyEnrichmentPIK3CB1.85
183Long qt syndromeEnrichmentCALM1, CALM21.80
184Costello syndromeEnrichmentHRAS1.78
185Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK1.78
186Encephalocraniocutaneous lipomatosisEnrichmentKRAS1.78
187Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC11.78
188Agammaglobulinemia, x-linkedEnrichmentBTK1.78
189Lymphoproliferative syndromeEnrichmentITK1.78
190Immunodeficiency 52EnrichmentLAT1.78
191Wooly hair nevusEnrichmentHRAS1.78
192Pelvic organ prolapseEnrichmentTAB21.73
193Proteasome-associated autoinflammatory syndrome 1EnrichmentPSMB41.73
194Gillespie syndromeEnrichmentITPR11.73
195Uvula, bifidEnrichmentUBB1.73
196Cleft soft palateEnrichmentUBB1.73
197Nasopharyngeal carcinomaEnrichmentNFKBIA1.73
198Proteosome-associated autoinflammatory syndromeEnrichmentPSMB41.73
199Frontometaphyseal dysplasiaEnrichmentMAP3K71.73
200Thyroid hemiagenesisEnrichmentPSMD31.73
201Thumb deformityEnrichmentCREBBP1.73
202Panbronchiolitis, diffuseEnrichmentMUC5B1.73
203Bleeding disorder, platelet-type, 19EnrichmentPRKACG1.73
204Menke-hennekam syndrome 2EnrichmentEP3001.73
205Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP1.73
206Fibrolamellar carcinomaEnrichmentPRKACA1.73
207Endometrial cancerEnrichmentPIK3CA1.64
208Hepatocellular carcinomaEnrichmentPIK3CA1.62
209Spinocerebellar ataxia 15EnrichmentITPR11.61
210Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK1.61
211Langerhans cell histiocytosisEnrichmentNRAS1.61
212Agammaglobulinemia 1EnrichmentBTK1.61
213SpermatocytomaEnrichmentHRAS1.61
214Non-immune hydrops fetalisEnrichmentHRAS, KRAS1.56
215Tethered spinal cord syndromeEnrichmentCREBBP1.56
216Intraocular pressure quantitative trait locusEnrichmentCREBBP1.56
217Lung cancerEnrichmentKRAS, PIK3CA1.54
218Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.51
219Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.51
220Prostate cancerEnrichmentPIK3CA1.50
221Cardiofaciocutaneous syndrome 1EnrichmentKRAS1.48
222Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS1.48
223Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.48
224Congenital generalized lipodystrophyEnrichmentFOS1.48
225Cardiofaciocutaneous syndromeEnrichmentKRAS1.48
226Lung sarcomatoid carcinomaEnrichmentKRAS1.48
227Pilocytic astrocytomaEnrichmentKRAS1.48
228Epidermolytic nevusEnrichmentHRAS1.48
229Knobloch syndromeEnrichmentPAK21.48
230Developmental dysplasia of the hip 1EnrichmentPSMC31.44
231Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.44
232Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR11.44
233Patent ductus arteriosusEnrichmentPSMC31.44
234Chronic mucocutaneous candidiasisEnrichmentCLEC7A1.44
235Noonan syndrome with multiple lentiginesEnrichmentRAF11.44
236Knobloch syndrome 1EnrichmentPAK21.39
237Histiocytoid hemangiomaEnrichmentFOS1.39
238MyelofibrosisEnrichmentSRC1.37
239Leukemia, acute myeloidEnrichmentKRAS, NRAS1.36
240Rubinstein-taybi syndrome 2EnrichmentEP3001.34
241Gastric cancerEnrichmentPIK3CA1.33
242Hereditary breast carcinomaEnrichmentPIK3CA1.32
243Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.31
244Ovarian cancerEnrichmentKRAS, MAP3K1, PIK3CA1.28
245Coronary heart disease 5EnrichmentIKBKG1.26
246Pulmonary fibrosisEnrichmentMUC5B1.26
247HypertrichosisEnrichmentCREBBP1.26
248HypertelorismEnrichmentPIK3CA1.25
249Myeloma, multipleEnrichmentPIK3R21.22
250PolymicrogyriaEnrichmentPSMC31.22
251Lennox-gastaut syndromeEnrichmentMAPK101.19
252Migraine with or without aura 1EnrichmentTAB21.18
253Congenital long qt syndromeEnrichmentITPR31.14
254Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.14
255Charge syndromeEnrichmentEP3001.09
256Multiple sclerosisEnrichmentITPR11.08
257OsteoporosisEnrichmentSRC1.08
25846,xy complete gonadal dysgenesisEnrichmentMAP3K11.06
259Specific learning disabilityEnrichmentMAPK11.06
260Anterior segment dysgenesisEnrichmentITPR11.05
261GliosarcomaEnrichmentNFKBIA1.02
262AsthmaEnrichmentMUC71.01
263Sudden infant death syndromeEnrichmentCALM21.00
264Giant cell glioblastomaEnrichmentNFKBIA1.00
265Protein-deficiency anemiaEnrichmentNRAS0.99
266MicrocephalyEnrichmentEP300, PAK3, PSMC30.97
267Complex neurodevelopmental disorderEnrichmentFBXW11, PAK3, PSMD120.96
268Lung cancer susceptibility 3EnrichmentKRAS0.96
269Cardiomyopathy, dilated, 1aEnrichmentNFATC20.91
270Heart diseaseEnrichmentCREBBP0.91
271RhabdomyosarcomaEnrichmentHRAS0.90
272Myocardial infarctionEnrichmentPSMA60.89
273Polydactyly, postaxial, type a1EnrichmentEP3000.88
274Corpus callosum, agenesis ofEnrichmentCREBBP0.88
275Isolated corpus callosum agenesisEnrichmentCREBBP0.88
276Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP0.88
277MalariaEnrichmentIKBKG0.88
278Heart, malformation ofEnrichmentMAPK10.85
279Interstitial lung disease 2EnrichmentMUC5B0.83
280Arteriovenous malformations of the brainEnrichmentKRAS0.83
281Diffuse large b-cell lymphomaEnrichmentBTK0.83
282Human immunodeficiency virus type 1EnrichmentCD2090.81
283Dilated cardiomyopathyEnrichmentRAF1, TAB20.77
284Severe combined immunodeficiencyEnrichmentIKBKB0.73
285Pancreatic cancerEnrichmentKRAS0.72
286Hydrops fetalis, nonimmuneEnrichmentHRAS0.71
287Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF10.70
288ScoliosisEnrichmentCREBBP0.70
289Severe covid-19EnrichmentMUC5B0.62
290ThrombocytopeniaEnrichmentSRC0.59
291Familial hypertrophic cardiomyopathyEnrichmentRAF10.58
292Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.57
293Left ventricular noncompactionEnrichmentRAF10.55
294Spastic ataxiaEnrichmentITPR10.55
295Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.53
296Hereditary breast ovarian cancer syndromeEnrichmentKRAS0.43
297Familial isolated dilated cardiomyopathyEnrichmentRAF10.41
298AutismEnrichmentCREBBP0.31
299Congenital nervous system abnormalityEnrichmentCREBBP0.20
300Nervous system diseaseEnrichmentCREBBP0.20

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