Immune response_Role of integrins in NK cells cytotoxicity

No Pathway Network information available for Immune response_Role of integrins in NK cells cytotoxicity

Pathways in the Immune response_Role of integrins in NK cells cytotoxicity SuperPath

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

Disorders associated with Immune response_Role of integrins in NK cells cytotoxicity SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1RasopathyEnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS1, SOS216.00
2Noonan syndrome 1EnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS1, SOS211.62
3Noonan syndrome and noonan-related syndromeEnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS111.11
4Noonan syndrome 3EnrichmentHRAS, PTPN11, RAF1, SOS18.47
5Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K24.21
6Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K24.21
7Noonan syndrome with multiple lentiginesEnrichmentPTPN11, RAF14.21
8Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.55
9Arteriovenous malformationEnrichmentHRAS, MAP2K13.44
10Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K13.34
11Lung non-small cell carcinomaEnrichmentHRAS, MAP2K13.26
12Specific learning disabilityEnrichmentMAPK1, PTPN113.26
1346,xy partial gonadal dysgenesisEnrichmentMAP3K1, SOS13.04
14Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN112.50
15MetachondromatosisEnrichmentPTPN112.49
16Systemic lupus erythematosus 6EnrichmentITGAM2.49
17Noonan syndrome 5EnrichmentRAF12.49
18Noonan syndrome 4EnrichmentSOS12.49
19Melorheostosis, isolatedEnrichmentMAP2K12.49
20Leopard syndrome 1EnrichmentPTPN112.49
21Cardiomyopathy, dilated, 1nnEnrichmentRAF12.49
22Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.49
23Noonan syndrome 9EnrichmentSOS22.49
2446,xy sex reversal 6EnrichmentMAP3K12.49
25Immunodeficiency 69EnrichmentIFNG2.49
26Noonan syndrome 13EnrichmentMAPK12.49
27Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.49
28MelorheostosisEnrichmentMAP2K12.49
29Leopard syndrome 2EnrichmentRAF12.49
30Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.49
31Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.49
32TrigonitisEnrichmentRAF12.49
33Vegetative pyoderma gangrenosumEnrichmentPTPN62.49
34Bullous pyoderma gangrenosumEnrichmentPTPN62.49
35Pustular pyoderma gangrenosumEnrichmentPTPN62.49
36Phakomatosis pigmentokeratoticaEnrichmentHRAS2.49
37Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.49
38Classic pyoderma gangrenosumEnrichmentPTPN62.49
39Malignant astrocytomaEnrichmentPTPN112.49
40Non-immune hydrops fetalisEnrichmentHRAS, PTPN112.35
41Leukocyte adhesion deficiency, type iEnrichmentITGB22.19
42Fibromatosis, gingival, 1EnrichmentSOS12.19
43Spondyloepimetaphyseal dysplasia, strudwick typeEnrichmentFN12.19
44Costello syndromeEnrichmentHRAS2.19
45Spondylometaphyseal dysplasia, corner fracture typeEnrichmentFN12.19
46Pulmonic stenosisEnrichmentSOS12.19
47Leukocyte adhesion deficiency, type iiiEnrichmentITGB22.19
48Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.19
49Werner syndromeEnrichmentPTPN112.19
50Tafro syndromeEnrichmentMAP2K22.19
51Wooly hair nevusEnrichmentHRAS2.19
52Tuberous sclerosis 1EnrichmentIFNG2.01
53Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG2.01
54Glomerulopathy with fibronectin deposits 2EnrichmentFN12.01
55Nuchal bleb, familialEnrichmentSOS12.01
56Langerhans cell histiocytosisEnrichmentMAP2K12.01
57Hepatitis c virusEnrichmentIFNG2.01
58Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.01
59Tuberous sclerosis 2EnrichmentIFNG2.01
60Large congenital melanocytic nevusEnrichmentHRAS2.01
61SpermatocytomaEnrichmentHRAS2.01
62Tricuspid valve insufficiencyEnrichmentPTPN112.01
63Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.89
64Autoimmune lymphoproliferative syndromeEnrichmentFASLG1.89
65Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.89
66Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.89
67Retinitis pigmentosa 26EnrichmentITGA41.89
68Congenital generalized lipodystrophyEnrichmentFOS1.89
69Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN111.89
70Epidermolytic nevusEnrichmentHRAS1.89
71Cerebral malariaEnrichmentICAM11.89
72Gingival fibromatosisEnrichmentSOS11.89
73Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.89
74LymphomaEnrichmentPTPN111.79
75Histiocytoid hemangiomaEnrichmentFOS1.79
76Idiopathic aplastic anemiaEnrichmentIFNG1.79
77Patent ductus arteriosusEnrichmentPTPN111.71
78Nevus, epidermalEnrichmentHRAS1.65
79Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.65
80Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.65
81Pilomyxoid astrocytomaEnrichmentRAF11.65
82Follicular thyroid carcinomaEnrichmentHRAS1.65
83Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.54
84Aplastic anemiaEnrichmentIFNG1.50
85Pectus excavatumEnrichmentPTPN111.45
8646,xy complete gonadal dysgenesisEnrichmentMAP3K11.45
87EpicanthusEnrichmentPTPN111.42
88Juvenile myelomonocytic leukemiaEnrichmentPTPN111.42
89Lip and oral cavity carcinomaEnrichmentHRAS1.42
90Congenital long qt syndromeEnrichmentPTPN111.42
91Aortic valve disease 1EnrichmentSOS11.38
92Neural tube defectsEnrichmentITGB11.38
93Isolated macular dystrophyEnrichmentITGA41.35
94Autism spectrum disorderEnrichmentMAP2K1, PTPN111.31
95RhabdomyosarcomaEnrichmentHRAS1.30
96Heart, malformation ofEnrichmentMAPK11.25
97Human immunodeficiency virus type 1EnrichmentIFNG1.25
98Patent foramen ovaleEnrichmentPTPN111.25
99MicrocephalyEnrichmentMAPK1, PTPN111.22
100MalariaEnrichmentICAM11.14
101Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.12
102ScoliosisEnrichmentPTPN111.12
103StrabismusEnrichmentPTPN111.08
104Bladder cancerEnrichmentHRAS1.05
105Differentiated thyroid carcinomaEnrichmentHRAS1.05
106Long qt syndrome 1EnrichmentPTPN111.03
107Lung cancerEnrichmentFASLG1.01
108Familial hypertrophic cardiomyopathyEnrichmentRAF10.99
109Left ventricular noncompactionEnrichmentRAF10.97
110Systemic lupus erythematosusEnrichmentITGAM0.92
111Nephrotic syndromeEnrichmentFN10.88
112Hypertrophic cardiomyopathyEnrichmentPTPN110.88
113ThrombocytopeniaEnrichmentPTPN110.84
114Familial isolated dilated cardiomyopathyEnrichmentRAF10.80
115Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.78
116Cone-rod dystrophy 2EnrichmentITGA40.70
117Breast cancerEnrichmentSHC10.66
118Dilated cardiomyopathyEnrichmentRAF10.64
119Ovarian cancerEnrichmentMAP3K10.55
120Inherited cancer-predisposing syndromeEnrichmentPTPN110.46
121Hereditary retinal dystrophyEnrichmentITGA40.21
122Fundus dystrophyEnrichmentITGA40.21

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