Antigen processing-Cross presentation

Pathway network for the Antigen processing-Cross presentation SuperPath

Sources:
  • Reactome

Pathways in the Antigen processing-Cross presentation SuperPath

Gene overlap in member pathways for Antigen processing-Cross presentation SuperPath

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

Disorders associated with Antigen processing-Cross presentation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Chronic granulomatous diseaseEnrichmentCYBA, CYBB, NCF1, NCF2, NCF410.26
2Immunodeficiency by defective expression of mhc class iEnrichmentB2M, TAP1, TAP2, TAPBP8.90
3Dysfibrinogenemia, congenitalEnrichmentFGA, FGB, FGG6.67
4Familial dysfibrinogenemiaEnrichmentFGA, FGB, FGG6.67
5Familial hypofibrinogenemiaEnrichmentFGA, FGB, FGG6.67
6Severe cutaneous adverse reactionEnrichmentHLA-A, HLA-B6.22
7Afibrinogenemia, congenitalEnrichmentFGA, FGB, FGG6.07
8Granulomatous disease, chronic, autosomal recessive, 2EnrichmentNCF1, NCF26.04
9Granulomatous disease, chronic, x-linkedEnrichmentCYBB, NCF15.74
10Proteasome-associated autoinflammatory syndrome 3EnrichmentPSMB4, PSMB94.44
11Proteasome-associated autoinflammatory syndrome 1EnrichmentPSMB4, PSMB83.97
12Proteosome-associated autoinflammatory syndromeEnrichmentPSMB4, PSMB83.97
13Mhc class i deficiency 1EnrichmentTAP1, TAP23.67
14Mhc class i deficiencyEnrichmentTAP1, TAP23.67
15MalariaEnrichmentCD36, IKBKG, TIRAP3.46
16Amyloidosis, hereditary systemic 2EnrichmentB2M, FGA3.45
17Granulomatous disease, chronic, autosomal recessive, 4EnrichmentCYBA3.23
18Immunodeficiency 34EnrichmentCYBB3.23
19Coronary heart disease 7EnrichmentCD363.23
20Platelet glycoprotein iv deficiencyEnrichmentCD363.23
21Immune dysregulation, neurodevelopmental defects, and colitisEnrichmentITGAV3.23
22Spondyloarthropathy 1EnrichmentHLA-B3.09
23Psoriasis 1EnrichmentHLA-C3.09
24Immunodeficiency 43EnrichmentB2M3.09
25Dialysis-related amyloidosisEnrichmentB2M3.09
26Ankylosing spondylitis 1EnrichmentHLA-B3.09
27Birdshot chorioretinopathyEnrichmentHLA-A3.09
28Reactive arthritisEnrichmentHLA-B3.09
29Amyloidosis, hereditary systemic 6EnrichmentB2M3.09
30Pulmonary arterial hypertension associated with connective tissue diseaseEnrichmentHLA-B3.09
31Granulomatous disease, chronic, autosomal recessive, 1EnrichmentNCF12.93
32Granulomatous disease, chronic, autosomal recessive, 3EnrichmentNCF42.93
33Stevens-johnson syndromeEnrichmentHLA-B2.79
34Autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasiaEnrichmentCYBA2.75
35Autoimmune polyendocrine syndrome type 1EnrichmentCYBA2.75
36Blood platelet diseaseEnrichmentCD362.63
37Cerebral malariaEnrichmentCD362.63
38Takayasu arteritisEnrichmentHLA-B2.61
39Temporal arteritisEnrichmentHLA-B2.49
40Cardiomyopathy, familial hypertrophic, 4EnrichmentNCF12.28
41B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentHLA-C2.25
42Behcet syndromeEnrichmentHLA-B, TLR42.24
43Diffuse large b-cell lymphomaEnrichmentBTK, MYD882.24
44Leprosy 3EnrichmentTLR22.22
45Incontinentia pigmentiEnrichmentIKBKG2.22
46Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.22
47Immunodeficiency 68EnrichmentMYD882.22
48Brachyphalangy, polydactyly, and tibial aplasia/hypoplasiaEnrichmentHMGB12.22
49Macroglobulinemia, waldenstrom 1EnrichmentMYD882.22
50Bacteremia 1EnrichmentTIRAP2.22
51Leprosy 5EnrichmentTLR12.22
52Fetal encasement syndromeEnrichmentCHUK2.22
53Immunodeficiency 15bEnrichmentIKBKB2.22
54Neurodevelopmental disorder with microcephaly, hypotonia, and absent languageEnrichmentPSMB12.22
55Immunodeficiency 15aEnrichmentIKBKB2.22
56Mhc class i deficiency 3EnrichmentTAPBP2.22
57Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.22
58Stankiewicz-isidor syndromeEnrichmentPSMD122.22
59Isolated growth hormone deficiency type iiiEnrichmentBTK2.22
60Tubulointerstitial kidney disease, autosomal dominant 5EnrichmentSEC61A12.22
61Deafness, cataract, impaired intellectual development, and polyneuropathyEnrichmentPSMC32.22
62Deafness, autosomal recessive 123EnrichmentSTX42.22
63Proteasome-associated autoinflammatory syndrome 6EnrichmentPSMB92.22
64Macular degeneration, age-related, 10EnrichmentTLR42.22
65Bartsocas-papas syndrome 2EnrichmentCHUK2.22
66Neutropenia, severe congenital, 11, autosomal dominantEnrichmentSEC61A12.22
67Congenital fibrinogen deficiencyEnrichmentFGG2.22
68Waldenstram macroglobulinemiaEnrichmentMYD882.22
69Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.22
70Lymphoma, non-hodgkin, familialEnrichmentB2M2.19
71Birbeck granule deficiencyEnrichmentCD2072.15
72AsthmaEnrichmentHLA-G2.05
73Williams-beuren syndromeEnrichmentNCF11.93
74Immunodeficiency 33EnrichmentIKBKG1.92
75Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK1.92
76Proteasome-associated autoinflammatory syndrome 5EnrichmentPSMB101.92
77Agammaglobulinemia, x-linkedEnrichmentBTK1.92
78Immunodeficiency, common variable, 15EnrichmentSEC61A11.92
79Immunodeficiency 121 with autoinflammationEnrichmentPSMB101.92
80Birk-aharoni syndromeEnrichmentPSMC11.92
81Leprosy 1EnrichmentTLR61.92
82Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG1.92
83Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG1.92
8417q24.2 microdeletion syndromeEnrichmentPSMD121.92
85Transient predisposition to invasive pyogenic bacterial infectionEnrichmentMYD881.92
86Submucosal cleft palateEnrichmentUBB1.92
87Cleft hard palateEnrichmentUBB1.92
88Human immunodeficiency virus type 1EnrichmentHLA-C1.84
89Severe covid-19EnrichmentITGAV1.77
90Thrombocythemia 1EnrichmentCALR1.74
91Uvula, bifidEnrichmentUBB1.74
92Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK1.74
93Cleft soft palateEnrichmentUBB1.74
94Agammaglobulinemia 1EnrichmentBTK1.74
95Thyroid hemiagenesisEnrichmentPSMD31.74
96Budd-chiari syndromeEnrichmentCALR1.62
97Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.52
98Developmental dysplasia of the hip 1EnrichmentPSMC31.45
99Patent ductus arteriosusEnrichmentPSMC31.45
100Thrombophilia due to thrombin defectEnrichmentFGA1.38
101MyelofibrosisEnrichmentCALR1.38
102Essential thrombocythemiaEnrichmentCALR1.38
103Spastic paraplegia 4, autosomal dominantEnrichmentFGG1.32
104Isolated split hand-split foot malformationEnrichmentSEM11.32
105Rheumatoid arthritisEnrichmentTLR11.27
106Coronary heart disease 5EnrichmentIKBKG1.27
107Omenn syndromeEnrichmentPSMB101.23
108PolymicrogyriaEnrichmentPSMC31.23
109Mhc class ii deficiency 1EnrichmentTAP21.19
110Polycystic liver diseaseEnrichmentSEC61A11.01
111Autosomal dominant polycystic liver diseaseEnrichmentSEC61A11.01
112Patent foramen ovaleEnrichmentPSMC30.99
113Myocardial infarctionEnrichmentPSMA60.90
114Multisystem inflammatory syndrome in childrenEnrichmentTLR60.90
115Autoinflammatory diseaseEnrichmentPSMB80.87
116Severe combined immunodeficiencyEnrichmentIKBKB0.74
117Sensorineural hearing lossEnrichmentSTX40.60
118ThrombocytopeniaEnrichmentFGG0.60
119Colorectal cancerEnrichmentTLR20.39
120MicrocephalyEnrichmentPSMC30.28
121Complex neurodevelopmental disorderEnrichmentPSMD120.28

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