CD209 (DC-SIGN) signaling

No Pathway Network information available for CD209 (DC-SIGN) signaling

Pathways in the CD209 (DC-SIGN) signaling SuperPath

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

Disorders associated with CD209 (DC-SIGN) signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome and noonan-related syndromeEnrichmentHRAS, KRAS, NRAS, RAF18.24
2Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS7.89
3Noonan syndrome 1EnrichmentHRAS, KRAS, NRAS, RAF17.43
4RasopathyEnrichmentHRAS, KRAS, NRAS, RAF17.21
5Nevus, epidermalEnrichmentHRAS, KRAS, NRAS6.95
6Noonan syndrome 3EnrichmentHRAS, KRAS, RAF16.95
7Melanocytic nevus syndrome, congenitalEnrichmentHRAS, NRAS, RAF16.75
8Lung non-small cell carcinomaEnrichmentHRAS, KRAS, NRAS6.28
9Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS5.64
10Large congenital melanocytic nevusEnrichmentHRAS, NRAS5.16
11Differentiated thyroid carcinomaEnrichmentHRAS, KRAS, NRAS4.94
12Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS4.86
13Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3004.47
14Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3004.47
15Thyroid cancer, nonmedullary, 2EnrichmentHRAS, NRAS4.32
16Leukemia, chronic myeloidEnrichmentKRAS, NRAS4.32
17Pilomyxoid astrocytomaEnrichmentKRAS, RAF14.32
18Follicular thyroid carcinomaEnrichmentHRAS, NRAS4.32
19Ellis-van creveld syndromeEnrichmentPRKACA, PRKACB4.09
20Juvenile myelomonocytic leukemiaEnrichmentKRAS, NRAS3.83
21Rare genetic intellectual disabilityEnrichmentCREBBP, EP3003.63
22Bladder cancerEnrichmentHRAS, KRAS3.04
23Non-immune hydrops fetalisEnrichmentHRAS, KRAS2.99
24Oculoectodermal syndromeEnrichmentKRAS2.81
25Intellectual developmental disorder, x-linked 30EnrichmentPAK32.81
26Noonan syndrome 5EnrichmentRAF12.81
27Cardiomyopathy, dilated, 1nnEnrichmentRAF12.81
28Melanosis, neurocutaneousEnrichmentNRAS2.81
29Noonan syndrome 6EnrichmentNRAS2.81
30Knobloch syndrome 2EnrichmentPAK22.81
31Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.81
32Cardioacrofacial dysplasia 2EnrichmentPRKACB2.81
33Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.81
34Leopard syndrome 2EnrichmentRAF12.81
35Dengue virusEnrichmentCD2092.81
36Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.81
37Cardioacrofacial dysplasia 1EnrichmentPRKACA2.81
38Immunodeficiency 53EnrichmentRELB2.81
39Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.81
40Menke-hennekam syndrome 1EnrichmentCREBBP2.81
41TrigonitisEnrichmentRAF12.81
42Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.81
43Congenital pulmonary airway malformationEnrichmentKRAS2.81
44Menke-hennekam syndromeEnrichmentCREBBP2.81
45Phakomatosis pigmentokeratoticaEnrichmentHRAS2.81
46Neurocutaneous melanocytosisEnrichmentNRAS2.81
47Leukemia, acute myeloidEnrichmentKRAS, NRAS2.76
48Costello syndromeEnrichmentHRAS2.51
49Thumb deformityEnrichmentCREBBP2.51
50Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.51
51Bleeding disorder, platelet-type, 19EnrichmentPRKACG2.51
52Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.51
53Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.51
54Menke-hennekam syndrome 2EnrichmentEP3002.51
55Rela fusion-positive ependymomaEnrichmentRELA2.51
56Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.51
57Fibrolamellar carcinomaEnrichmentPRKACA2.51
58Common variable immunodeficiency 12EnrichmentNFKB12.51
59Wooly hair nevusEnrichmentHRAS2.51
60Myeloma, multipleEnrichmentCREBBP, KRAS2.48
61Langerhans cell histiocytosisEnrichmentNRAS2.33
62Tethered spinal cord syndromeEnrichmentCREBBP2.33
63Intraocular pressure quantitative trait locusEnrichmentCREBBP2.33
64SpermatocytomaEnrichmentHRAS2.33
65Cardiofaciocutaneous syndrome 1EnrichmentKRAS2.21
66Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS2.21
67Cardiofaciocutaneous syndromeEnrichmentKRAS2.21
68Lung sarcomatoid carcinomaEnrichmentKRAS2.21
69Noonan syndrome with multiple lentiginesEnrichmentRAF12.21
70Pilocytic astrocytomaEnrichmentKRAS2.21
71Epidermolytic nevusEnrichmentHRAS2.21
72Knobloch syndromeEnrichmentPAK22.21
73Knobloch syndrome 1EnrichmentPAK22.11
74Rubinstein-taybi syndrome 2EnrichmentEP3002.11
75Colorectal cancerEnrichmentEP300, NRAS2.10
76Breast adenocarcinomaEnrichmentKRAS2.03
77Lung squamous cell carcinomaEnrichmentKRAS2.03
78HypertrichosisEnrichmentCREBBP2.03
79Capillary malformation-arteriovenous malformation 1EnrichmentKRAS1.97
80Gallbladder cancerEnrichmentKRAS1.97
81Common variable immunodeficiencyEnrichmentNFKB11.97
82Charge syndromeEnrichmentEP3001.86
83Arteriovenous malformationEnrichmentHRAS1.86
84MicrocephalyEnrichmentEP300, PAK31.82
85Myopathy, x-linked, with excessive autophagyEnrichmentHRAS1.81
86Ciliary dyskinesia, primary, 3EnrichmentNFKB11.81
87Lip and oral cavity carcinomaEnrichmentHRAS1.73
88Protein-deficiency anemiaEnrichmentNRAS1.70
89Lung cancer susceptibility 3EnrichmentKRAS1.67
90Heart diseaseEnrichmentCREBBP1.67
91Polydactyly, postaxial, type a1EnrichmentEP3001.64
92Corpus callosum, agenesis ofEnrichmentCREBBP1.64
93Lynch syndromeEnrichmentKRAS1.64
94Isolated corpus callosum agenesisEnrichmentCREBBP1.64
95Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.64
96RhabdomyosarcomaEnrichmentHRAS1.61
97Human immunodeficiency virus type 1EnrichmentCD2091.56
98Arteriovenous malformations of the brainEnrichmentKRAS1.54
99Diffuse large b-cell lymphomaEnrichmentCREBBP1.54
100Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.44
101ScoliosisEnrichmentCREBBP1.44
102Pancreatic cancerEnrichmentKRAS1.42
103Hydrops fetalis, nonimmuneEnrichmentHRAS1.40
104Lung cancerEnrichmentKRAS1.31
105Familial hypertrophic cardiomyopathyEnrichmentRAF11.30
106Left ventricular noncompactionEnrichmentRAF11.28
107Gastric cancerEnrichmentKRAS1.19
108Hereditary breast carcinomaEnrichmentKRAS1.18
109Familial isolated dilated cardiomyopathyEnrichmentRAF11.10
110Hereditary breast ovarian cancer syndromeEnrichmentKRAS1.09
111AutismEnrichmentCREBBP0.98
112Breast cancerEnrichmentKRAS0.96
113Dilated cardiomyopathyEnrichmentRAF10.93
114Ovarian cancerEnrichmentKRAS0.84
115Congenital nervous system abnormalityEnrichmentCREBBP0.82
116Nervous system diseaseEnrichmentCREBBP0.82
117Complex neurodevelopmental disorderEnrichmentPAK30.76

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