Immune response CD16 signaling in NK cells

No Pathway Network information available for Immune response CD16 signaling in NK cells

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

Disorders associated with Immune response CD16 signaling in NK cells SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1RasopathyEnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS1, SOS210.98
2Noonan syndrome 1EnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS1, SOS210.57
3Noonan syndrome and noonan-related syndromeEnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS110.27
4Noonan syndrome 3EnrichmentHRAS, PTPN11, RAF1, SOS17.83
5Arteriovenous malformationEnrichmentHRAS, MAP2K1, PIK3CA5.10
6Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K1, PIK3CA4.95
7Lung non-small cell carcinomaEnrichmentHRAS, MAP2K1, PIK3CA4.81
8Wiskott-aldrich syndromeEnrichmentWAS, WIPF14.67
9Baraitser-winter cerebrofrontofacial syndromeEnrichmentACTB, ACTG14.67
10Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM1, CALM2, CALM34.61
11Immunoglobulin kappa light chain deficiencyEnrichmentIGK, IGKC4.23
12Immune system diseaseEnrichmentCDC42, PIK3CD4.23
13Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.20
14Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R14.20
15Immunodeficiency 14EnrichmentPIK3CD, PIK3R14.20
16Long qt syndrome 1EnrichmentCALM1, CALM2, CALM3, ITPR34.10
17Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K23.90
18Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R23.90
19Chromosome 22q11.2 deletion syndrome, distalEnrichmentCRKL, MAPK13.90
20Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K23.90
21Noonan syndrome with multiple lentiginesEnrichmentPTPN11, RAF13.90
22Recurrent infections associated with rare immunoglobulin isotypes deficiencyEnrichmentIGK, IGKC3.75
23Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCBL, CDC423.45
24Pseudomyogenic hemangioendotheliomaEnrichmentACTB, FOSB3.45
25Nevus, epidermalEnrichmentHRAS, PIK3CA3.36
26Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K1, PIK3CA3.36
27Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.23
28Histiocytoid hemangiomaEnrichmentFOS, FOSB3.23
29Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD, PIK3R13.03
30Combined immunodeficiencyEnrichmentARPC1B, ZAP702.94
31Combined t cell and b cell immunodeficiencyEnrichmentARPC1B, ZAP702.94
32Specific learning disabilityEnrichmentMAPK1, PTPN112.94
33Combined t and b cell immunodeficiencyEnrichmentARPC1B, ZAP702.94
34Lip and oral cavity carcinomaEnrichmentHRAS, PIK3CA2.87
35Severe combined immunodeficiencyEnrichmentCD247, LCK, ZAP702.68
36MicrocephalyEnrichmentACTB, ACTG1, MAPK1, PTPN112.60
37Breast cancerEnrichmentIL2, JUN, PIK3CA, SHC12.57
38MacrodactylyEnrichmentPIK3CA2.33
39Spondyloarthropathy 1EnrichmentHLA-B2.33
40MetachondromatosisEnrichmentPTPN112.33
41Baraitser-winter syndrome 1EnrichmentACTB2.33
42Thrombocytopenia 1EnrichmentWAS2.33
43Noonan syndrome 5EnrichmentRAF12.33
44Noonan syndrome 4EnrichmentSOS12.33
45Psoriasis 1EnrichmentHLA-C2.33
46Melorheostosis, isolatedEnrichmentMAP2K12.33
47Megalencephaly, autosomal dominantEnrichmentPIK3CA2.33
48Leopard syndrome 1EnrichmentPTPN112.33
49Cardiomyopathy, dilated, 1nnEnrichmentRAF12.33
50Cowden syndrome 5EnrichmentPIK3CA2.33
51Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.33
52Noonan syndrome 9EnrichmentSOS22.33
53Wiskott-aldrich syndrome 2EnrichmentWIPF12.33
54Cerebral cavernous malformations 4EnrichmentPIK3CA2.33
55Noonan syndrome 13EnrichmentMAPK12.33
56Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.33
57Immunodeficiency 48EnrichmentZAP702.33
58Short syndromeEnrichmentPIK3R12.33
59Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.33
60Congenital smooth muscle hamartoma, with or without hemihypertrophyEnrichmentACTB2.33
61Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.33
62Immunodeficiency 71 with inflammatory disease and congenital thrombocytopeniaEnrichmentARPC1B2.33
63Ankylosing spondylitis 1EnrichmentHLA-B2.33
64Hemifacial myohyperplasiaEnrichmentPIK3CA2.33
65Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.33
66Becker nevus syndromeEnrichmentACTB2.33
67MelorheostosisEnrichmentMAP2K12.33
68Dystonia-deafness syndrome 1EnrichmentACTB2.33
69Leopard syndrome 2EnrichmentRAF12.33
70Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.33
71Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.33
72Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.33
73Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.33
74Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.33
75Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.33
76Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.33
77Reactive arthritisEnrichmentHLA-B2.33
78Immunodeficiency 22EnrichmentLCK2.33
79Was-related disordersEnrichmentWAS2.33
80Thrombocytopenia 8, with dysmorphic features and developmental delayEnrichmentACTB2.33
81TrigonitisEnrichmentRAF12.33
82Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.33
83Baraitser-winter syndromeEnrichmentACTB2.33
84HypospadiasEnrichmentPIK3CA2.33
85ColitisEnrichmentSYK2.33
86Rare venous malformationEnrichmentPIK3CA2.33
87Vegetative pyoderma gangrenosumEnrichmentPTPN62.33
88Bullous pyoderma gangrenosumEnrichmentPTPN62.33
89Diaphragmatic eventrationEnrichmentPIK3CA2.33
90Congenital smooth muscle hamartomaEnrichmentACTB2.33
91Pustular pyoderma gangrenosumEnrichmentPTPN62.33
92Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.33
93Developmental malformations-deafness-dystonia syndromeEnrichmentACTB2.33
94Pulmonary arterial hypertension associated with connective tissue diseaseEnrichmentHLA-B2.33
95Rare combined vascular malformationEnrichmentPIK3CA2.33
96Cavernous lymphangiomaEnrichmentPIK3CA2.33
97Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.33
98Phakomatosis pigmentokeratoticaEnrichmentHRAS2.33
99Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.33
100Classic pyoderma gangrenosumEnrichmentPTPN62.33
101Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.33
102Eccrine angiomatous hamartomaEnrichmentPIK3CA2.33
103Macrodactyly of toeEnrichmentPIK3CA2.33
104Zap70-related severe combined immunodeficiencyEnrichmentZAP702.33
105Malignant astrocytomaEnrichmentPTPN112.33
106Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN112.19
107RhabdomyosarcomaEnrichmentCBL, HRAS2.18
108Anhidrosis, isolated, with normal sweat glandsEnrichmentITPR22.11
109Mitochondrial myopathy with lactic acidosisEnrichmentPNPLA82.11
110Osteopetrosis and infantile neuroaxonal dystrophyEnrichmentPLA2G62.11
111Cardiac valvular dysplasia 1EnrichmentPLD12.11
112Fleck retina, familial benignEnrichmentPLA2G52.11
113Immunodeficiency 20EnrichmentFCGR3A2.11
114Immunodeficiency 69EnrichmentIFNG2.11
115Neurodegeneration with brain iron accumulation 2aEnrichmentPLA2G62.11
116Charcot-marie-tooth disease, demyelinating, type 1jEnrichmentITPR32.11
117Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.11
118Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.11
119Immunodeficiency 25EnrichmentCD2472.11
120Parkinson disease 14, autosomal recessiveEnrichmentPLA2G62.11
121Neurodegeneration with brain iron accumulation 2bEnrichmentPLA2G62.11
122Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorderEnrichmentPLA2G4A2.11
123Long qt syndrome 16EnrichmentCALM32.11
124Platelet-activating factor acetylhydrolase deficiencyEnrichmentPLA2G72.11
125Gastrointestinal ulceration, recurrent, with dysfunctional plateletsEnrichmentPLA2G4A2.11
126Takenouchi-kosaki syndromeEnrichmentCDC422.11
127Long qt syndrome 15EnrichmentCALM22.11
128Immunodeficiency 133 with ectodermal dysplasia with or without peripheral neuropathyEnrichmentITPR32.11
129B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)EnrichmentIGH2.11
130Nocarh syndromeEnrichmentCDC422.11
131Aplasia cutis-enamel dysplasia syndromeEnrichmentFOSL22.11
132Cryptogenic multifocal ulcerous stenosing enteritisEnrichmentPLA2G4A2.11
133Familial benign flecked retinaEnrichmentPLA2G52.11
134Bladder cancerEnrichmentHRAS, PIK3CA2.10
135Non-immune hydrops fetalisEnrichmentHRAS, PTPN112.04
136Fibromatosis, gingival, 1EnrichmentSOS12.03
137Costello syndromeEnrichmentHRAS2.03
138Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1EnrichmentTYROBP2.03
139Neutropenia, severe congenital, x-linkedEnrichmentWAS2.03
140Severe cutaneous adverse reactionEnrichmentHLA-B2.03
141Pulmonic stenosisEnrichmentSOS12.03
142Deafness, autosomal dominant 20EnrichmentACTG12.03
143Keratosis, seborrheicEnrichmentPIK3CA2.03
144Roifman-chitayat syndromeEnrichmentPIK3CD2.03
145Baraitser-winter syndrome 2EnrichmentACTG12.03
146Noonan syndrome 8EnrichmentPIK3CA2.03
147Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.03
148Developmental delay, language impairment, and ocular abnormalitiesEnrichmentARPC42.03
149Werner syndromeEnrichmentPTPN112.03
150Stevens-johnson syndromeEnrichmentHLA-B2.03
151Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.03
152Immunodeficiency 113 with autoimmunity and autoinflammationEnrichmentARPC52.03
153Immunodeficiency 52EnrichmentLAT2.03
154ArthritisEnrichmentSYK2.03
155Immunodeficiency 133EnrichmentARPC52.03
156Tafro syndromeEnrichmentMAP2K22.03
157Wooly hair nevusEnrichmentHRAS2.03
158Takayasu arteritisEnrichmentHLA-B1.86
159Pompe disease, infantile-onsetEnrichmentPIK3CA1.86
160Nuchal bleb, familialEnrichmentSOS11.86
161Langerhans cell histiocytosisEnrichmentMAP2K11.86
162Neutrophilic dermatosis, acute febrileEnrichmentPTPN61.86
163Large congenital melanocytic nevusEnrichmentHRAS1.86
164SpermatocytomaEnrichmentHRAS1.86
165Tricuspid valve insufficiencyEnrichmentPTPN111.86
166KeratoacanthomaEnrichmentPIK3CA1.86
167Spinocerebellar ataxia 29EnrichmentITPR11.81
168Ovarian germ cell cancerEnrichmentCBL1.81
169Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM11.81
170Long qt syndrome 14EnrichmentCALM11.81
171Immunodeficiency 127EnrichmentTNF1.81
172Intellectual developmental disorder, autosomal dominant 60, with seizuresEnrichmentPIP5K1A1.81
173Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC21.81
174Malignant germ cell tumor of ovaryEnrichmentCBL1.81
175Infantile osteopetrosis with neuroaxonal dysplasiaEnrichmentPLA2G61.81
176Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.73
177Temporal arteritisEnrichmentHLA-B1.73
178Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.73
179Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R21.73
180Aminoacylase 1 deficiencyEnrichmentACTB1.73
181Cerebrovascular diseaseEnrichmentPIK3CA1.73
182Epidermolytic nevusEnrichmentHRAS1.73
183Familial cerebral cavernous malformationsEnrichmentPIK3CA1.73
184Gingival fibromatosisEnrichmentSOS11.73
185Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.73
186ThrombocytopeniaEnrichmentPTPN11, WAS1.68
187Capillary malformations, congenitalEnrichmentPIK3CA1.64
188LymphomaEnrichmentPTPN111.64
189HemimegalencephalyEnrichmentPIK3CA1.64
190Coloboma of choroid and retinaEnrichmentACTG11.64
191Gillespie syndromeEnrichmentITPR11.64
192Tuberous sclerosis 1EnrichmentIFNG1.64
193Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG1.64
194Agammaglobulinemia 1, autosomal recessiveEnrichmentIGH1.64
195Late-onset retinal degenerationEnrichmentPLA2G51.64
196Psoriatic arthritisEnrichmentTNF1.64
197Hepatitis c virusEnrichmentIFNG1.64
198Tuberous sclerosis 2EnrichmentIFNG1.64
199Agammaglobulinemia 1EnrichmentIGH1.64
200Migraine without auraEnrichmentTNF1.64
201T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD2471.64
202Long qt syndromeEnrichmentCALM1, CALM21.62
203Lung cancerEnrichmentFASLG, PIK3CA1.60
204Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.56
205Cowden syndrome 1EnrichmentPIK3CA1.56
206Hemihyperplasia, isolatedEnrichmentPIK3CA1.56
207Patent ductus arteriosusEnrichmentPTPN111.56
208Breast adenocarcinomaEnrichmentPIK3CA1.56
209Lung squamous cell carcinomaEnrichmentPIK3CA1.56
210Colorectal cancerEnrichmentPIK3CA, PIK3R1, PLA2G2A1.52
211Autoimmune lymphoproliferative syndromeEnrichmentFASLG1.51
212Spinocerebellar ataxia 15EnrichmentITPR11.51
213Congenital generalized lipodystrophyEnrichmentFOS1.51
214Mantle cell lymphomaEnrichmentIGH1.51
215Cerebral malariaEnrichmentTNF1.51
216Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.49
217Gallbladder cancerEnrichmentPIK3CA1.49
218Pilomyxoid astrocytomaEnrichmentRAF11.49
219Follicular thyroid carcinomaEnrichmentHRAS1.49
220Overgrowth syndromeEnrichmentPIK3R11.49
221B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentHLA-C1.49
222Systemic lupus erythematosusEnrichmentIGHG1, TNF1.44
223Lymphoma, mucosa-associated lymphoid typeEnrichmentIGH1.42
224Follicular lymphomaEnrichmentIGH1.42
225Myeloproliferative neoplasmEnrichmentCBL1.42
226Vascular dementiaEnrichmentTNF1.42
227Aggressive systemic mastocytosisEnrichmentCBL1.42
228Idiopathic aplastic anemiaEnrichmentIFNG1.42
229Inflammatory bowel disease 1EnrichmentPRKCQ1.39
230Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.39
231Adult hepatocellular carcinomaEnrichmentPIK3CA1.39
232Cowden syndromeEnrichmentPIK3CA1.39
233Cat eye syndromeEnrichmentACTG11.34
234Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.34
235Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR11.34
236Pectus excavatumEnrichmentPTPN111.30
237Immune deficiency diseaseEnrichmentSYK1.30
238AsthmaEnrichmentHLA-G1.30
239Oligoarticular juvenile idiopathic arthritisEnrichmentCD2471.28
240Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD2471.28
241EpicanthusEnrichmentPTPN111.26
242Juvenile myelomonocytic leukemiaEnrichmentPTPN111.26
243MeningiomaEnrichmentPIK3CA1.26
244Congenital long qt syndromeEnrichmentPTPN111.26
245Aortic valve disease 1EnrichmentSOS11.23
246Nk-cell enteropathyEnrichmentPIK3CB1.23
247Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.22
24846,xy partial gonadal dysgenesisEnrichmentSOS11.20
249Spastic ataxiaEnrichmentITPR1, PLA2G61.20
250Lynch syndromeEnrichmentPIK3CA1.17
251Leukemia, chronic lymphocyticEnrichmentIGHG11.13
252Aplastic anemiaEnrichmentIFNG1.13
253Neurodegeneration with brain iron accumulationEnrichmentPLA2G61.13
254Familial colorectal cancerEnrichmentPLA2G2A1.13
255Heart, malformation ofEnrichmentMAPK11.09
256Human immunodeficiency virus type 1EnrichmentHLA-C1.09
257Patent foramen ovaleEnrichmentPTPN111.09
258Behcet syndromeEnrichmentHLA-B1.07
259Autism spectrum disorderEnrichmentMAP2K1, PTPN111.04
260Endometrial cancerEnrichmentPIK3CA1.03
261LissencephalyEnrichmentACTG11.03
262Alzheimer's diseaseEnrichmentTNF1.02
263Hepatocellular carcinomaEnrichmentPIK3CA1.01
264Multiple sclerosisEnrichmentITPR10.99
265Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF10.98
266ScoliosisEnrichmentPTPN110.98
267Anterior segment dysgenesisEnrichmentITPR10.96
268Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delayEnrichmentPLA2G60.93
269StrabismusEnrichmentPTPN110.93
270Sudden infant death syndromeEnrichmentCALM20.91
271Prostate cancerEnrichmentPIK3CA0.90
272Differentiated thyroid carcinomaEnrichmentHRAS0.90
273Familial hypertrophic cardiomyopathyEnrichmentRAF10.85
274CakutEnrichmentACTG10.83
275Left ventricular noncompactionEnrichmentRAF10.82
276Cardiomyopathy, dilated, 1aEnrichmentNFATC20.82
277Non-syndromic genetic deafnessEnrichmentACTG10.81
278MalariaEnrichmentTNF0.79
279Nonsyndromic hearing lossEnrichmentACTG10.75
280Gastric cancerEnrichmentPIK3CA0.74
281Hypertrophic cardiomyopathyEnrichmentPTPN110.74
282Hereditary breast carcinomaEnrichmentPIK3CA0.73
283HypertelorismEnrichmentPIK3CA0.67
284Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentACTG10.67
285Familial isolated dilated cardiomyopathyEnrichmentRAF10.66
286Myeloma, multipleEnrichmentPIK3R20.64
287Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.64
288Rare genetic deafnessEnrichmentACTG10.51
289Dilated cardiomyopathyEnrichmentRAF10.51
290Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.49
291Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.45
292Ovarian cancerEnrichmentPIK3CA0.42
293Inherited cancer-predisposing syndromeEnrichmentPTPN110.34
294Congenital nervous system abnormalityEnrichmentPLA2G60.25
295Nervous system diseaseEnrichmentPLA2G60.25

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