BAFF in B-Cell Signaling

Pathway network for the BAFF in B-Cell Signaling SuperPath

Sources:
  • QIAGEN
  • GeneGo (Thomson Reuters)

Pathways in the BAFF in B-Cell Signaling SuperPath

#NameSourceGenes
1BAFF in B-Cell SignalingQIAGEN
2RANK Signaling in OsteoclastsQIAGEN
3Apoptosis and survival APRIL and BAFF signalingGeneGo (Thomson Reuters)
4APRIL PathwayQIAGEN
5RANK PathwayQIAGEN

Gene overlap in member pathways for BAFF in B-Cell Signaling SuperPath

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

Disorders associated with BAFF in B-Cell Signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome and noonan-related syndromeEnrichmentBRAF, CBL, MAP2K1, MAP2K2, RAF18.53
2Noonan syndrome 1EnrichmentBRAF, CBL, MAP2K1, MAP2K2, RAF17.50
3RasopathyEnrichmentBRAF, CBL, MAP2K1, MAP2K2, RAF17.21
4Cardiofaciocutaneous syndrome 1EnrichmentBRAF, MAP2K1, MAP2K26.58
5Cardiofaciocutaneous syndromeEnrichmentBRAF, MAP2K1, MAP2K26.58
6Common variable immunodeficiencyEnrichmentNFKB1, NFKB2, TNFRSF13B6.08
7Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA5.52
8Immunodeficiency, common variable, 2EnrichmentCR2, TNFRSF13B5.07
9Langerhans cell histiocytosisEnrichmentBRAF, MAP2K14.30
10Immunodeficiency, common variable, 1EnrichmentNFKB2, TNFRSF13B4.30
11Noonan syndrome with multiple lentiginesEnrichmentBRAF, RAF14.00
12Pilomyxoid astrocytomaEnrichmentBRAF, RAF13.46
13Melanocytic nevus syndrome, congenitalEnrichmentBRAF, RAF13.34
14MelanomaEnrichmentBRAF, MITF3.13
15Lung non-small cell carcinomaEnrichmentBRAF, MAP2K13.05
16Myeloma, multipleEnrichmentBRAF, PIK3R2, TRAF52.80
17Incontinentia pigmentiEnrichmentIKBKG2.75
18Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.75
19Osteopetrosis, autosomal recessive 7EnrichmentTNFRSF11A2.75
20Fetal encasement syndromeEnrichmentCHUK2.75
21Ataxia-oculomotor apraxia 3EnrichmentPIK3R52.75
22Immunodeficiency 15bEnrichmentIKBKB2.75
23Immunodeficiency 15aEnrichmentIKBKB2.75
24Short syndromeEnrichmentPIK3R12.75
25Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.75
26Immunodeficiency 132aEnrichmentTRAF32.75
27Immunodeficiency 132bEnrichmentTRAF32.75
28Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.75
29Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.75
30Thrombocytopenia 6EnrichmentSRC2.75
31Bartsocas-papas syndrome 2EnrichmentCHUK2.75
32Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.75
33Melanoma, cutaneous malignant 1EnrichmentBRAF, MITF2.66
34Immune deficiency, familial variableEnrichmentTNFRSF13B2.56
35Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.56
36Frontometaphyseal dysplasia 2EnrichmentMAP3K72.56
37Immunoglobulin a deficiency 2EnrichmentTNFRSF13B2.56
38Immunodeficiency 112EnrichmentMAP3K142.56
39Common variable immunodeficiency phenotype due to homozygous taci deficiencyEnrichmentTNFRSF13B2.56
40Inflammatory bowel disease-recurrent sinopulmonary infections syndromeEnrichmentNFAT52.56
41Nik deficiencyEnrichmentMAP3K142.56
4246,xy sex reversal 6EnrichmentMAP3K12.53
43Congenital disorder of glycosylation, type iizEnrichmentCAMLG2.53
44Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.53
45Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.53
46Graft-versus-host diseaseEnrichmentIL102.53
47Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.53
48Immunodeficiency 53EnrichmentRELB2.53
49Familial expansile osteolysisEnrichmentTNFRSF11A2.45
50Paget disease of bone 5, juvenile-onsetEnrichmentTNFRSF11A2.45
51Ovarian germ cell cancerEnrichmentCBL2.45
52Immunodeficiency 33EnrichmentIKBKG2.45
53Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2EnrichmentPIK3R52.45
54Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.45
55Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.45
56Osteopetrosis, autosomal recessive 2EnrichmentTNFSF112.45
57Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.45
58Malignant germ cell tumor of ovaryEnrichmentCBL2.45
59Common variable immunodeficiency 12EnrichmentNFKB12.45
60Pallister-killian syndromeEnrichmentARAF2.38
61Lymphoproliferative syndrome, x-linked, 2EnrichmentXIAP2.38
62Noonan syndrome 5EnrichmentRAF12.38
63Melorheostosis, isolatedEnrichmentMAP2K12.38
64Noonan syndrome 7EnrichmentBRAF2.38
65Leopard syndrome 3EnrichmentBRAF2.38
66Amyloidosis, finnish typeEnrichmentGSN2.38
67Heterochromia iridisEnrichmentMITF2.38
68Tietz albinism-deafness syndromeEnrichmentMITF2.38
69Cardiomyopathy, dilated, 1nnEnrichmentRAF12.38
70Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.38
71Noonan syndrome 13EnrichmentMAPK12.38
72Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafnessEnrichmentMITF2.38
73LymphangiomaEnrichmentBRAF2.38
74Phace associationEnrichmentBRAF2.38
75MelorheostosisEnrichmentMAP2K12.38
76Leopard syndrome 2EnrichmentRAF12.38
77Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.38
78TrigonitisEnrichmentRAF12.38
79Cerebral cavernous malformations 5EnrichmentMAP3K32.38
80Syringocystadenoma papilliferumEnrichmentBRAF2.38
81GangliogliomaEnrichmentBRAF2.38
82Nongerminomatous germ cell tumorEnrichmentBRAF2.38
83Phace syndromeEnrichmentBRAF2.38
84Classic hairy cell leukemiaEnrichmentBRAF2.38
85Verrucous hemangiomaEnrichmentMAP3K32.38
86Polyvalvular heart disease syndromeEnrichmentTAB22.38
87Dilated cardiomyopathyEnrichmentBRAF, RAF1, TAB22.36
88DysosteosclerosisEnrichmentTNFRSF11A2.28
89Nasopharyngeal carcinomaEnrichmentNFKBIA2.28
90Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3R12.28
91Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.28
92Immunodeficiency 14EnrichmentPIK3R12.28
93Adult-onset myasthenia gravisEnrichmentTNFRSF11A2.28
94Immunodeficiency with hyper-igm, type 2EnrichmentTNFRSF13B2.26
95Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.26
96Colorectal cancerEnrichmentBRAF, PIK3R1, SRC2.26
97Immunodeficiency, common variable, 4EnrichmentTNFRSF13C2.25
98Systemic lupus erythematosusEnrichmentCR2, IL102.23
99Osteogenesis imperfecta, type ixEnrichmentPPIB2.23
100Immunodeficiency, common variable, 10EnrichmentNFKB22.23
101Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.23
102Intravascular large b-cell lymphomaEnrichmentBCL22.23
103Immunodeficiency, common variable, 7EnrichmentCR22.23
104Rela fusion-positive ependymomaEnrichmentRELA2.23
105Paget disease of bone 2, early-onsetEnrichmentTNFRSF11A2.15
106Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3R22.15
107Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R22.15
108Congenital generalized lipodystrophyEnrichmentFOS2.15
109Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCBL2.15
110Autosomal recessive osteopetrosisEnrichmentTNFSF112.15
111Paget's disease of bone 2EnrichmentTNFRSF11A2.15
112Frontometaphyseal dysplasiaEnrichmentMAP3K72.09
113Pulmonic stenosisEnrichmentBRAF2.08
114Melanoma, cutaneous malignant 8EnrichmentMITF2.08
115Papillary renal cell carcinomaEnrichmentMITF2.08
116Congenital heart defects, multiple types, 2EnrichmentTAB22.08
117Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.08
118Tafro syndromeEnrichmentMAP2K22.08
119Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.05
120Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG2.05
121Myeloproliferative neoplasmEnrichmentCBL2.05
122Histiocytoid hemangiomaEnrichmentFOS2.05
123Herpes simplex virus encephalitisEnrichmentTRAF32.05
124Aggressive systemic mastocytosisEnrichmentCBL2.05
125Systemic lupus erythematosus 9EnrichmentCR22.05
126High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL22.05
127MyelofibrosisEnrichmentSRC1.91
128Overgrowth syndromeEnrichmentPIK3R11.91
129Pelvic organ prolapseEnrichmentTAB21.91
130Ataxia-telangiectasiaEnrichmentBRAF1.91
131Waardenburg syndrome, type 2aEnrichmentMITF1.91
132Tethered spinal cord syndromeEnrichmentBRAF1.91
133Follicular lymphomaEnrichmentBCL21.83
134Coronary heart disease 5EnrichmentIKBKG1.80
135Thyroid cancer, nonmedullary, 1EnrichmentBRAF1.78
136Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.78
137Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.78
138Lymphoproliferative syndrome 2EnrichmentXIAP1.78
139CraniopharyngiomaEnrichmentBRAF1.78
140Newborn respiratory distress syndromeEnrichmentBRAF1.78
141Clear cell papillary renal cell carcinomaEnrichmentMITF1.78
142Ciliary dyskinesia, primary, 3EnrichmentNFKB11.76
143Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.76
144Il10-related early-onset inflammatory bowel diseaseEnrichmentIL101.76
145Osteogenesis imperfecta, type iiEnrichmentPPIB1.69
146Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC31.69
147Juvenile myelomonocytic leukemiaEnrichmentCBL1.68
148Lennox-gastaut syndromeEnrichmentMAPK101.67
149OsteoporosisEnrichmentSRC1.61
150Waardenburg syndrome, type 4aEnrichmentMITF1.61
151Wilms tumor 5EnrichmentBRAF1.61
152Waardenburg syndromeEnrichmentMITF1.61
153Rheumatoid arthritisEnrichmentIL101.58
154RhabdomyosarcomaEnrichmentCBL1.55
155GliosarcomaEnrichmentNFKBIA1.55
156Thyroid cancer, nonmedullary, 2EnrichmentBRAF1.54
157Waardenburg syndrome, type 1EnrichmentMITF1.54
158Waardenburg syndrome, type 2eEnrichmentMITF1.54
159Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.54
160Noonan syndrome 3EnrichmentRAF11.54
161Gallbladder cancerEnrichmentBRAF1.54
162Follicular thyroid carcinomaEnrichmentBRAF1.54
163Giant cell glioblastomaEnrichmentNFKBIA1.53
16446,xy complete gonadal dysgenesisEnrichmentMAP3K11.50
165Lymphoma, non-hodgkin, familialEnrichmentBRAF1.49
166Cardiomyopathy, familial hypertrophic, 4EnrichmentBRAF1.44
167Arteriovenous malformationEnrichmentMAP2K11.44
168Primary hyperaldosteronismEnrichmentBRAF1.44
169Ventricular septal defectEnrichmentBRAF1.44
170Osteogenesis imperfecta, type ivEnrichmentPPIB1.42
171Multisystem inflammatory syndrome in childrenEnrichmentTRAF31.42
172MalariaEnrichmentIKBKG1.40
17346,xy partial gonadal dysgenesisEnrichmentMAP3K11.39
174Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.39
175Osteogenesis imperfecta, type iiiEnrichmentPPIB1.36
176Migraine with or without aura 1EnrichmentTAB21.35
177Specific learning disabilityEnrichmentMAPK11.35
178Lip and oral cavity carcinomaEnrichmentBRAF1.31
179Human immunodeficiency virus type 1EnrichmentIL101.29
180Aortic valve disease 1EnrichmentTAB21.28
181Behcet syndromeEnrichmentIL101.26
182Cardiomyopathy, dilated, 1aEnrichmentNFATC21.25
183Lung cancer susceptibility 3EnrichmentBRAF1.25
184Severe combined immunodeficiencyEnrichmentIKBKB1.25
185Wilms tumor 1EnrichmentBRAF1.22
186Brittle bone disorderEnrichmentPPIB1.18
187Dandy-walker syndromeEnrichmentBRAF1.17
188Heart, malformation ofEnrichmentMAPK11.14
189Patent foramen ovaleEnrichmentTAB21.14
190Arteriovenous malformations of the brainEnrichmentBRAF1.12
191Diffuse large b-cell lymphomaEnrichmentBRAF1.12
192ThrombocytopeniaEnrichmentSRC1.09
193Ear malformationEnrichmentMITF1.02
194Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.02
195Autoinflammatory diseaseEnrichmentXIAP1.02
196Differentiated thyroid carcinomaEnrichmentBRAF0.95
197Lung cancerEnrichmentBRAF0.91
198Breast cancerEnrichmentJUN0.90
199Familial hypertrophic cardiomyopathyEnrichmentRAF10.89
200Left ventricular noncompactionEnrichmentRAF10.87
201Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.86
202Non-syndromic genetic deafnessEnrichmentMITF0.86
203Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.82
204Nonsyndromic hearing lossEnrichmentMITF0.80
205Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentMITF0.71
206Familial isolated dilated cardiomyopathyEnrichmentRAF10.71
207Hereditary breast ovarian cancer syndromeEnrichmentMITF0.69
208Ovarian cancerEnrichmentMAP3K10.59
209Rare genetic deafnessEnrichmentMITF0.55
210Autism spectrum disorderEnrichmentMAP2K10.44
211MicrocephalyEnrichmentMAPK10.40
212Inherited cancer-predisposing syndromeEnrichmentMITF0.37

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