Modulators of TCR signaling and T cell activation

No Pathway Network information available for Modulators of TCR signaling and T cell activation

Pathways in the Modulators of TCR signaling and T cell activation SuperPath

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

Disorders associated with Modulators of TCR signaling and T cell activation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Neurodevelopmental disorder with motor and speech delay and behavioral abnormalitiesEnrichmentTMEM2222.73
2Lymphoproliferative syndrome, x-linked, 1EnrichmentSH2D1A2.73
3Rhabdoid tumor predisposition syndrome 1EnrichmentSMARCB12.73
4Neuroendocrine tumorEnrichmentCDKN1B2.73
5NeurilemmomaEnrichmentSMARCB12.73
6Coffin-siris syndrome 3EnrichmentSMARCB12.73
7Thauvin-robinet-faivre syndromeEnrichmentFIBP2.73
8Immunodeficiency 129EnrichmentRHOH2.73
9Learning disabilityEnrichmentFIBP2.73
10Familial behcet-like autoinflammatory syndromeEnrichmentTNFAIP32.73
11T-cell immunodeficiency with epidermodysplasia verruciformisEnrichmentRHOH2.73
12Vegetative pyoderma gangrenosumEnrichmentPTPN62.73
13Bullous pyoderma gangrenosumEnrichmentPTPN62.73
14Pustular pyoderma gangrenosumEnrichmentPTPN62.73
15Classic pyoderma gangrenosumEnrichmentPTPN62.73
16Systemic lupus erythematosusEnrichmentSOCS1, TNFAIP32.63
17Schwannomatosis 1EnrichmentSMARCB12.43
18Autoinflammatory syndrome, familial, behcet-like 1EnrichmentTNFAIP32.43
19Multiple endocrine neoplasia, type ivEnrichmentCDKN1B2.43
20Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizuresEnrichmentAGO12.43
21Rhabdoid tumor predisposition syndromeEnrichmentSMARCB12.43
22Lymphoproliferative syndromeEnrichmentSH2D1A2.43
23Immune thrombocytopeniaEnrichmentSOCS12.26
24Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.26
25Autoinflammatory syndrome, familial, with or without immunodeficiencyEnrichmentSOCS12.26
26Atypical teratoid rhabdoid tumorEnrichmentSMARCB12.26
27Mitochondrial complex i deficiency, nuclear type 35EnrichmentNDUFB102.26
28SchwannomatosisEnrichmentSMARCB12.26
29Anemia, autoimmune hemolyticEnrichmentSOCS12.13
30Primary hyperparathyroidismEnrichmentCDKN1B2.13
31Full schwannomatosisEnrichmentSMARCB12.13
32Multiple endocrine neoplasia, type iEnrichmentCDKN1B1.89
33Overgrowth syndromeEnrichmentFIBP1.89
34Ovarian cancerEnrichmentCDKN1B, SMARCB11.83
35Autism spectrum disorderEnrichmentARIH2, SMARCB11.77
36Meningioma, familialEnrichmentSMARCB11.70
37Complex neurodevelopmental disorderEnrichmentAGO1, TMEM2221.66
38MeningiomaEnrichmentSMARCB11.66
39Microphthalmia/coloboma 12EnrichmentFIBP1.63
40Nk-cell enteropathyEnrichmentSMARCB11.63
41Inherited cancer-predisposing syndromeEnrichmentCDKN1B, SMARCB11.61
42Coloboma of maculaEnrichmentFIBP1.56
43Coffin-siris syndrome 1EnrichmentSMARCB11.56
44Diffuse large b-cell lymphomaEnrichmentSOCS11.46
45Noonan syndrome 1EnrichmentRASA21.38
46Autoinflammatory diseaseEnrichmentSH2D1A1.36
47Mitochondrial complex i deficiency, nuclear type 1EnrichmentNDUFB101.17

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