Immune response Lectin induced complement pathway

Pathway network for the Immune response Lectin induced complement pathway SuperPath

Sources:
  • GeneGo (Thomson Reuters)
  • Reactome

Pathways in the Immune response Lectin induced complement pathway SuperPath

#NameSourceGenes
1Immune response Lectin induced complement pathwayGeneGo (Thomson Reuters)
2Immune response Classical complement pathwayGeneGo (Thomson Reuters)
3Immune response Alternative complement pathwayGeneGo (Thomson Reuters)
4Terminal pathway of complementReactome

Gene overlap in member pathways for Immune response Lectin induced complement pathway SuperPath

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

Disorders associated with Immune response Lectin induced complement pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Immunodeficiency due to a classical component pathway complement deficiencyEnrichmentC1QA, C1QB, C1QC, C1R, C1S, C2, C4A, C4B11.22
2Immunodeficiency due to a late component of complement deficiencyEnrichmentC5, C6, C7, C8A, C8B, C8G, C910.58
3Atypical hemolytic uremic syndrome with complement gene abnormalityEnrichmentC3, CD46, CFB, CFH, CFI10.40
4Genetic atypical hemolytic-uremic syndromeEnrichmentC3, CD46, CFH8.31
5Atypical hemolytic-uremic syndromeEnrichmentC3, CD46, CFH, CFI7.99
6Hellp syndromeEnrichmentCD46, CFH, CFI7.71
7C1q deficiency 1EnrichmentC1QA, C1QB, C1QC7.50
8Systemic lupus erythematosusEnrichmentC4A, C4B, CR2, IGHG1, ITGAM6.82
9Complement component 6 deficiencyEnrichmentC6, C8B6.52
10Systemic lupus erythematosus 16EnrichmentC1QA, C1R, C4A6.50
11De novo thrombotic microangiopathy after kidney transplantationEnrichmentCFH, CFI5.52
12Familial drusenEnrichmentCFH, CFI5.05
13Immunoglobulin kappa light chain deficiencyEnrichmentIGK, IGKC4.99
14Periodontal ehlers-danlos syndromeEnrichmentC1R, C1S4.99
15Hemolytic uremic syndrome, atypical 1EnrichmentC3AR1, CFH4.52
16Ehlers-danlos syndrome, periodontal type, 1EnrichmentC1R, C1S4.51
17Agammaglobulinemia 1, autosomal recessiveEnrichmentIGH, IGHM4.51
18Agammaglobulinemia 1EnrichmentIGH, IGHM4.51
19Ehlers-danlos syndrome, periodontal type, 2EnrichmentC1R, C1S4.51
20Recurrent infections associated with rare immunoglobulin isotypes deficiencyEnrichmentIGK, IGKC4.51
21Complement component 5 deficiencyEnrichmentC53.23
22Complement component 7 deficiencyEnrichmentC73.23
23Complement component 8 deficiency, type iEnrichmentC8A3.23
24Macular degeneration, age-related, 15EnrichmentC93.23
25Eculizumab, poor response toEnrichmentC53.23
26Complement component 9 deficiencyEnrichmentC93.23
27Complement component 8 deficiency, type iiEnrichmentC8B3.23
28LathosterolosisEnrichmentC52.93
29Systemic lupus erythematosus 6EnrichmentITGAM2.75
30Basal laminar drusenEnrichmentCFH2.75
31Hemolytic uremic syndrome, atypical 4EnrichmentCFB2.75
32Complement factor d deficiencyEnrichmentCFD2.75
33Macular degeneration, age-related, 4EnrichmentCFH2.75
34Hemolytic uremic syndrome, atypical 5EnrichmentC32.75
35Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathyEnrichmentCD552.75
36Blood group, cromer systemEnrichmentCD552.75
37Hemolytic uremic syndrome, atypical 3EnrichmentCFI2.75
38Macular degeneration, age-related, 13EnrichmentCFI2.75
39Properdin deficiency, x-linkedEnrichmentCFP2.75
40Complement factor h deficiencyEnrichmentCFH2.75
41Complement factor i deficiencyEnrichmentCFI2.75
42Hemolytic uremic syndrome, atypical 2EnrichmentCD462.75
43Hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathyEnrichmentCD592.75
44Macular degeneration, age-related, 9EnrichmentC32.75
45Complement component 3 deficiency, autosomal recessiveEnrichmentC32.75
46Complement factor b deficiencyEnrichmentCFB2.75
47Complement component 3 deficiencyEnrichmentC32.75
48Membranoproliferative glomerulonephritisEnrichmentC32.75
49Primary membranoproliferative glomerulonephritisEnrichmentC32.75
50Protein-losing enteropathyEnrichmentCD552.75
51Genetic hemolytic uremic syndromeEnrichmentCFH2.75
52Recurrent neisseria infections due to factor d deficiencyEnrichmentCFD2.75
53Immunodeficiency with factor h anomalyEnrichmentCFH2.75
54Complement component 4, partial deficiency ofEnrichmentSERPING12.63
553mc syndrome 1EnrichmentMASP12.63
56Complement component 2 deficiencyEnrichmentC22.63
57Ficolin 3 deficiencyEnrichmentFCN32.63
58Complement component 4a deficiencyEnrichmentC4A2.63
59Blood group, chido/rodgers systemEnrichmentC4A2.63
60Complement component 4b deficiencyEnrichmentC4B2.63
61Masp2 deficiencyEnrichmentMASP22.63
62Mannose-binding lectin deficiencyEnrichmentMBL22.63
63C1 inhibitor deficiencyEnrichmentSERPING12.63
64Rheumatic heart diseaseEnrichmentFCN32.63
65Immunodeficiency due to ficolin3 deficiencyEnrichmentFCN32.63
66Hereditary angioedema with c1inh deficiencyEnrichmentSERPING12.63
67Immunodeficiency due to masp-2 deficiencyEnrichmentMASP22.63
68C1q deficiency 3EnrichmentC1QC2.49
69C1q deficiency 2EnrichmentC1QB2.49
70B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)EnrichmentIGH2.49
71Leukocyte adhesion deficiency, type iEnrichmentITGB22.45
72Cyclic neutropeniaEnrichmentCFD2.45
73Immunodeficiency, common variable, 2EnrichmentCR22.45
74Leukocyte adhesion deficiency, type iiiEnrichmentITGB22.45
75Macular degeneration, age-related, 14EnrichmentCFB2.45
76Immunodeficiency, common variable, 7EnrichmentCR22.45
77Nephrotic syndrome, type 7EnrichmentCFH2.45
78AngioedemaEnrichmentSERPING12.33
79Neutropenia, severe congenital, 1, autosomal dominantEnrichmentCFD2.28
80Systemic lupus erythematosus 9EnrichmentCR22.28
81Complement component c1s deficiencyEnrichmentC1S2.19
82Afibrinogenemia, congenitalEnrichmentCFI2.15
83Thrombotic microangiopathyEnrichmentCD462.15
84Angioedema, hereditary, 1EnrichmentSERPING12.15
85C3 glomerulopathyEnrichmentCFH2.05
86Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentMASP21.93
87Mantle cell lymphomaEnrichmentIGH1.89
883mc syndromeEnrichmentMASP11.85
89Lymphoma, mucosa-associated lymphoid typeEnrichmentIGH1.79
90Follicular lymphomaEnrichmentIGH1.79
91Chronic kidney diseaseEnrichmentCFH1.64
92Leukemia, chronic lymphocyticEnrichmentIGHG11.50
93Autosomal non-syndromic agammaglobulinemiaEnrichmentIGHM1.50
94MalariaEnrichmentCR11.40
95Behcet syndromeEnrichmentC4A1.36
96Ehlers-danlos syndromeEnrichmentC1R1.22
97Severe covid-19EnrichmentFCN21.18
98Cystic fibrosisEnrichmentMBL21.14
99Hereditary retinal dystrophyEnrichmentCFH0.39
100Fundus dystrophyEnrichmentCFH0.39

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