Cellular Senescence

Pathway network for the Cellular Senescence SuperPath

Sources:
  • Reactome

Pathways in the Cellular Senescence SuperPath

#NameSourceGenes
1Cellular SenescenceReactome
2Oxidative Stress Induced SenescenceReactome
3Senescence-Associated Secretory Phenotype (SASP)Reactome

Gene overlap in member pathways for Cellular Senescence SuperPath

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

Disorders associated with Cellular Senescence SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Melanoma, cutaneous malignant 1EnrichmentACD, CDK4, CDKN2A, CDKN2B, POT1, TERF2IP7.12
2Multiple endocrine neoplasia, type iEnrichmentCDKN1A, CDKN1B, CDKN2B, CDKN2C6.84
3Tessadori-bicknell-van haaften neurodevelopmental syndrome 4EnrichmentH2BC12, H4C1, H4C96.27
4Inherited cancer-predisposing syndromeEnrichmentATM, CDK4, CDKN1B, CDKN2A, EZH2, MRE11, NBN, POT1, RAD50, RB1, TP535.62
5Dedifferentiated liposarcomaEnrichmentCDK4, HMGA2, MDM25.57
6Well-differentiated liposarcomaEnrichmentCDK4, HMGA2, MDM25.57
7Li-fraumeni syndromeEnrichmentCDKN2A, MDM2, TP534.84
8Glioma susceptibility 1EnrichmentH3-3A, H3C1, TP534.39
9Bladder cancerEnrichmentATM, CDKN1A, CDKN2A, RB1, TP534.34
10Tessadori-bicknell-van haaften neurodevelopmental syndrome 1EnrichmentH4C1, H4C34.18
11Tessadori-bicknell-van haaften neurodevelopmental syndrome 2EnrichmentH4C1, H4C114.18
12Bryant-li-bhoj neurodevelopmental syndrome 2EnrichmentH3-3A, H3-3B4.18
13Breast cancerEnrichmentATM, CDKN2B, JUN, MRE11, NBN, RAD50, TP534.08
14Ovarian cancerEnrichmentATM, CDKN1B, CDKN2A, MRE11, NBN, RAD50, RB1, TP534.07
15Tessadori-bicknell-van haaften neurodevelopmental syndrome 3EnrichmentH4C1, H4C53.70
16Weaver syndromeEnrichmentEZH2, SUZ123.61
17Leukemia, chronic lymphocyticEnrichmentATM, POT1, TP533.52
18Gastric cancerEnrichmentATM, CDK4, CDKN2A, NBN, TP533.50
19Pancreatic cancerEnrichmentATM, CDKN2A, NBN, TP533.43
20Lip and oral cavity carcinomaEnrichmentCDKN2A, RB1, TP533.27
21Osteogenic sarcomaEnrichmentRB1, TP533.24
22Squamous cell carcinomaEnrichmentRB1, TP533.24
23AdenocarcinomaEnrichmentATM, TP533.24
24Bone osteosarcomaEnrichmentRB1, TP533.24
25Complex neurodevelopmental disorderEnrichmentAGO1, H4C3, H4C5, H4C9, RNF2, TNRC6B3.02
26Hereditary breast ovarian cancer syndromeEnrichmentATM, MRE11, NBN, RAD50, TP533.00
27Myeloma, multipleEnrichmentATM, CDKN2C, ERF, H3C1, TP532.96
28Small cell cancer of the lungEnrichmentRB1, TP532.94
29Nijmegen breakage syndrome-like disorderEnrichmentMRE11, RAD502.94
30Adrenocortical carcinomaEnrichmentCDKN2A, TP532.92
31B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentCDKN2A, TP532.77
32Diffuse large b-cell lymphomaEnrichmentNBN, STAT3, TP532.65
33Hoyeraal-hreidarsson syndromeEnrichmentACD, TINF22.55
34Hereditary breast carcinomaEnrichmentATM, NBN, RAD50, TP532.49
35Hepatocellular carcinomaEnrichmentNBN, RAD50, TP532.47
36Specific learning disabilityEnrichmentMAPK1, RPS6KA32.46
37Colonic benign neoplasmEnrichmentATM, MRE112.18
38Prostate cancerEnrichmentATM, NBN, TP532.12
39Coffin-lowry syndromeEnrichmentRPS6KA32.09
40Melanoma, cutaneous malignant 3EnrichmentCDK42.09
41Microcephaly 12, primary, autosomal recessiveEnrichmentCDK62.09
42Noonan syndrome 13EnrichmentMAPK12.09
43Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA32.09
44T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.09
45Ferguson-bonni neurodevelopmental syndromeEnrichmentANAPC72.09
46Developmental and epileptic encephalopathy 109EnrichmentFZR12.09
47Rothmund-thomson syndrome, type 1EnrichmentANAPC12.09
48Neuroendocrine tumorEnrichmentCDKN1B2.09
49Retinal arterial macroaneurysm with supravalvular pulmonic stenosisEnrichmentIGFBP72.09
50Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.09
51Bryant-li-bhoj neurodevelopmental syndrome 1EnrichmentH3-3A2.09
52Cdkn2a cancer predispositionEnrichmentCDKN2A2.09
53Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA32.09
54Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.09
55Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.09
56Spermatogenic failure, x-linked, 9EnrichmentRBBP72.04
5746,xy sex reversal 5EnrichmentCBX22.04
58Microcephaly 11, primary, autosomal recessiveEnrichmentPHC12.04
59Accelerated tumor formationEnrichmentMDM22.04
60Global developmental delay with speech and behavioral abnormalitiesEnrichmentTNRC6B2.04
61Luo-schoch-yamamoto syndromeEnrichmentRNF22.04
62Lessel-kubisch syndromeEnrichmentMDM22.04
63Bone marrow failure syndrome 6EnrichmentMDM42.04
64Bone marrow failure syndrome 5EnrichmentTP532.04
65Papilloma of choroid plexusEnrichmentTP532.04
66Basal cell carcinoma 7EnrichmentTP532.04
67Imagawa-matsumoto syndromeEnrichmentSUZ122.04
68Anaplastic thyroid carcinomaEnrichmentTP532.04
69Intellectual developmental disorder, autosomal recessive 54EnrichmentTNIK2.04
70Neurocardiofaciodigital syndromeEnrichmentMAPKAPK52.04
71Macular dystrophy, patterned, 3EnrichmentMAPKAPK32.04
72Ductal carcinoma in situEnrichmentTP532.04
73Epilepsy, familial adult myoclonic, 6EnrichmentTNRC6A2.04
74Cohen-gibson syndromeEnrichmentEED2.04
75Thyroid gland undifferentiated carcinomaEnrichmentTP532.04
76Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.04
77Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.04
78Choroid plexus cancerEnrichmentTP532.04
79Pleomorphic xanthoastrocytomaEnrichmentTP532.04
80Leukemia, acute lymphoblasticEnrichmentCDKN2A, NBN2.01
81Breast-ovarian cancer, familial 1EnrichmentATM, NBN1.86
82Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typicalEnrichmentLMNB11.85
83Craniosynostosis 4EnrichmentERF1.85
84Tumor predisposition syndrome 3EnrichmentPOT11.85
85Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8EnrichmentPOT11.85
86Silver-russell syndrome 5EnrichmentHMGA21.85
87Adult onset demyelinating leukodystrophyEnrichmentLMNB11.85
88Ataxia-telangiectasia-like disorder 1EnrichmentMRE111.85
89Stature quantitative trait locus 9EnrichmentHMGA21.85
90High-grade astrocytoma with piloid featuresEnrichmentPOT11.85
91Cerebroretinal microangiopathy with calcifications and cysts 3EnrichmentPOT11.85
92Microcephaly 26, primary, autosomal dominantEnrichmentLMNB11.85
93Endometrial serous adenocarcinomaEnrichmentATM1.85
94Chitayat syndromeEnrichmentERF1.85
95Trilateral retinoblastomaEnrichmentRB11.85
96B-cell non-hodgkin lymphomaEnrichmentATM1.85
97Lung oat cell carcinomaEnrichmentRB11.85
98Lung cancer susceptibility 3EnrichmentRB1, TP531.80
99Melanoma-astrocytoma syndromeEnrichmentCDKN2A1.79
100Scoliosis, isolated 1EnrichmentMAPK71.79
101Melanoma, cutaneous malignant 2EnrichmentCDKN2A1.79
102Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB11.79
103Multiple endocrine neoplasia, type ivEnrichmentCDKN1B1.79
104Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA1.79
105Rela fusion-positive ependymomaEnrichmentRELA1.79
106Kleefstra syndromeEnrichmentEHMT11.79
107Melanoma-pancreatic cancer syndromeEnrichmentCDKN2A1.79
108Kleefstra syndrome due to a point mutationEnrichmentEHMT11.79
109Common variable immunodeficiency 12EnrichmentNFKB11.79
110Submucosal cleft palateEnrichmentUBB1.79
111Cleft hard palateEnrichmentUBB1.79
112Adrenocortical carcinoma, hereditaryEnrichmentTP531.74
113Cervical cancerEnrichmentTP531.74
114Lymphoma, hodgkin, classicEnrichmentTP531.74
115Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizuresEnrichmentAGO11.74
116Congenital fibrosarcomaEnrichmentTP531.74
117Li-fraumeni syndrome 1EnrichmentTP531.74
118SarcomaEnrichmentTP531.74
119Cervix carcinomaEnrichmentTP531.74
120Hodgkin's lymphomaEnrichmentTP531.74
121Stolerman neurodevelopmental syndromeEnrichmentKDM6B1.74
122Pleomorphic rhabdomyosarcomaEnrichmentTP531.74
123GliosarcomaEnrichmentATM, TP531.69
124Giant cell glioblastomaEnrichmentATM, TP531.64
125Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT31.61
126Uvula, bifidEnrichmentUBB1.61
127Cleft soft palateEnrichmentUBB1.61
128Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT31.61
129Hyper ige syndromeEnrichmentSTAT31.61
130Nasopharyngeal carcinomaEnrichmentTP531.57
131Anus, imperforateEnrichmentMAP4K41.57
132Bacteremia 2EnrichmentMAPKAPK31.57
133Atypical teratoid rhabdoid tumorEnrichmentTP531.57
134Anaplastic astrocytomaEnrichmentTP531.57
135Revesz syndromeEnrichmentTINF21.56
136Salivary gland adenoma, pleomorphicEnrichmentHMGA21.56
137Chromosome 13q14 deletion syndromeEnrichmentRB11.56
138Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalitiesEnrichmentKAT51.56
139Cardiac valvular dysplasia, x-linkedEnrichmentATM1.56
140Dyskeratosis congenita, autosomal dominant 3EnrichmentTINF21.56
141OligodendrogliomaEnrichmentPOT11.56
142High grade gliomaEnrichmentATM1.56
143Autosomal dominant primary microcephalyEnrichmentLMNB11.56
144T-cell prolymphocytic leukemiaEnrichmentATM1.56
145Anaplastic oligodendrogliomaEnrichmentPOT11.56
14612q14 microdeletion syndromeEnrichmentHMGA21.56
147Familial retinoblastomaEnrichmentRB11.56
148Arteriovenous malformations of the brainEnrichmentIL6, MAP4K41.54
149Dyskeratosis congenitaEnrichmentPOT1, TINF21.54
150Kaposi sarcomaEnrichmentIL61.49
151Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.49
152Congenital generalized lipodystrophyEnrichmentFOS1.49
153Primary hyperparathyroidismEnrichmentCDKN1B1.49
154Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.49
155Primary autosomal recessive microcephalyEnrichmentCDK6, PHC11.46
156Thyroid cancer, nonmedullary, 1EnrichmentTP531.44
157Lung sarcomatoid carcinomaEnrichmentTP531.44
158Embryonal rhabdomyosarcomaEnrichmentTP531.44
159TuberculosisEnrichmentMAPKAPK31.44
160Rheumatoid arthritis, systemic juvenileEnrichmentIL61.40
161Deafness, autosomal recessive 63EnrichmentANAPC151.40
162Histiocytoid hemangiomaEnrichmentFOS1.40
163Crouzon syndromeEnrichmentERF1.38
164Craniosynostosis 1EnrichmentERF1.38
165Jacobsen syndromeEnrichmentETS11.38
166RetinoblastomaEnrichmentRB11.38
167Ataxia-telangiectasiaEnrichmentATM1.38
168Nijmegen breakage syndromeEnrichmentNBN1.38
169Polycythemia veraEnrichmentATM1.38
170Woolly hair, autosomal recessive 3EnrichmentRB11.38
171Dyskeratosis congenita, autosomal dominant 6EnrichmentACD1.38
172Hypotrichosis 8EnrichmentRB11.38
173Koolen-de vries syndromeEnrichmentATM1.38
174Rhabdomyosarcoma 2EnrichmentTP531.35
175Myasthenic syndrome, congenital, 4a, slow-channelEnrichmentMINK11.35
176LymphomaEnrichmentTP531.35
177Myasthenic syndrome, congenital, 4b, fast-channelEnrichmentMINK11.35
178Acute megakaryocytic leukemiaEnrichmentTP531.35
179Endometrial stromal sarcomaEnrichmentSUZ121.35
180Type 1 diabetes mellitusEnrichmentIL61.32
181Kleefstra syndrome 1EnrichmentEHMT11.32
182Lung squamous cell carcinomaEnrichmentCDKN2A1.32
183Breast adenocarcinomaEnrichmentTP531.27
184Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemiaEnrichmentMRE111.26
185Lynch syndrome 4EnrichmentRB11.26
186Mantle cell lymphomaEnrichmentATM1.26
187Silver-russell syndrome due to a point mutationEnrichmentHMGA21.26
188Oculomotor apraxiaEnrichmentATM1.26
189Common variable immunodeficiencyEnrichmentNFKB11.25
190Esophageal cancerEnrichmentTP531.21
191Squamous cell carcinoma, head and neckEnrichmentTP531.21
192Myasthenic syndrome, congenital, 1a, slow-channelEnrichmentMINK11.21
193Essential thrombocythemiaEnrichmentTP531.21
194Gallbladder cancerEnrichmentTP531.21
195Gastroesophageal refluxEnrichmentRPS6KA31.20
196Orthostatic intoleranceEnrichmentRPS6KA31.20
197Permanent neonatal diabetes mellitusEnrichmentSTAT31.20
198GlioblastomaEnrichmentATM1.17
199Renal hypodysplasia/aplasia 1EnrichmentMAP4K41.15
200Lymphoma, non-hodgkin, familialEnrichmentTP531.15
201Lennox-gastaut syndromeEnrichmentMAPK101.15
202Inflammatory bowel disease 1EnrichmentIL61.15
203Ventricular septal defectEnrichmentRPS6KA31.15
204Ciliary dyskinesia, primary, 3EnrichmentNFKB11.10
205PolymicrogyriaEnrichmentEHMT11.10
206MelanomaEnrichmentCDKN2A1.10
207Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentTNRC6B1.10
208Adult hepatocellular carcinomaEnrichmentTP531.10
209Primary hyperaldosteronismEnrichmentTP531.10
210Dyskeratosis congenita, autosomal dominant 1EnrichmentTINF21.09
211Clear cell renal cell carcinomaEnrichmentATM1.09
212Myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiencyEnrichmentMINK11.06
213Familial colorectal cancerEnrichmentTP531.06
214Silver-russell syndrome 1EnrichmentHMGA21.03
215Renal cell carcinoma, papillary, 1EnrichmentATM1.03
216Dyskeratosis congenita, autosomal dominant 2EnrichmentTINF21.03
217Myelodysplastic syndromeEnrichmentTP531.02
21846,xy complete gonadal dysgenesisEnrichmentCBX21.02
219Acute promyelocytic leukemiaEnrichmentSTAT30.99
220Type 2 diabetes mellitusEnrichmentHMGA1, IL60.93
221Congenital myasthenic syndromeEnrichmentMINK10.92
222Lynch syndrome 1EnrichmentATM0.88
223Aplastic anemiaEnrichmentNBN0.88
224RhabdomyosarcomaEnrichmentTP530.86
225Isolated congenital microcephalyEnrichmentPHC10.86
226Heart, malformation ofEnrichmentMAPK10.86
227Immune deficiency diseaseEnrichmentATM0.84
228Uterine corpus cancerEnrichmentATM0.84
229Familial colorectal cancer type xEnrichmentATM0.84
230Digeorge syndromeEnrichmentHIRA0.81
231Premature menopauseEnrichmentNBN0.78
232Precursor t-cell acute lymphoblastic leukemiaEnrichmentCDKN2A0.76
233HepatoblastomaEnrichmentTP530.76
234Multisystem inflammatory syndrome in childrenEnrichmentIFNB10.74
235Diamond-blackfan anemia 1EnrichmentTP530.72
236MalariaEnrichmentMAPKAPK30.72
237Renal cell carcinoma, nonpapillaryEnrichmentATM0.72
238Autism spectrum disorderEnrichmentEED, EHMT1, TNRC6B0.71
239Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA30.59
240Endometrial cancerEnrichmentATM0.59
241LissencephalyEnrichmentNBN0.59
242Diamond-blackfan anemiaEnrichmentTP530.55
243Leukemia, acute myeloidEnrichmentTP530.51
244Colorectal cancerEnrichmentATM, TP530.46
245HypertelorismEnrichmentRPS6KA30.46
246Non-immune hydrops fetalisEnrichmentUBN10.45
247Undetermined early-onset epileptic encephalopathyEnrichmentFZR10.43
248SchizophreniaEnrichmentEHMT10.41
249Autosomal recessive non-syndromic intellectual disabilityEnrichmentTNIK0.38
250Systemic lupus erythematosusEnrichmentETS10.37
251MicrocephalyEnrichmentMAPK1, NBN0.29
252Primary ovarian insufficiencyEnrichmentNBN0.25

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