TP53 Regulates Transcription of Cell Death Genes

Pathway network for the TP53 Regulates Transcription of Cell Death Genes SuperPath

Sources:
  • Reactome

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

Disorders associated with TP53 Regulates Transcription of Cell Death Genes SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1AdenocarcinomaEnrichmentATM, TP536.04
2Gastric cancerEnrichmentATM, CASP10, TP535.78
3Lymphoma, non-hodgkin, familialEnrichmentCASP10, TP535.07
4Leukemia, chronic lymphocyticEnrichmentATM, TP534.86
5Myeloma, multipleEnrichmentATM, CREBBP, TP534.63
6GliosarcomaEnrichmentATM, TP534.44
7Giant cell glioblastomaEnrichmentATM, TP534.39
8Pancreatic cancerEnrichmentATM, TP534.04
9Bladder cancerEnrichmentATM, TP533.91
10Prostate cancerEnrichmentATM, TP533.91
11Familial cold autoinflammatory syndrome 4EnrichmentNLRC43.83
12Autoinflammation with infantile enterocolitisEnrichmentNLRC43.83
13Periodic fever-infantile enterocolitis-autoinflammatory syndromeEnrichmentNLRC43.83
14Diffuse large b-cell lymphomaEnrichmentCREBBP, TP533.78
15Hereditary breast carcinomaEnrichmentATM, TP533.55
16Bone marrow failure syndrome 5EnrichmentTP533.43
17Papilloma of choroid plexusEnrichmentTP533.43
18Basal cell carcinoma 7EnrichmentTP533.43
19Anaplastic thyroid carcinomaEnrichmentTP533.43
20Ductal carcinoma in situEnrichmentTP533.43
21Thyroid gland undifferentiated carcinomaEnrichmentTP533.43
22Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP533.43
23Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP533.43
24Choroid plexus cancerEnrichmentTP533.43
25Pleomorphic xanthoastrocytomaEnrichmentTP533.43
26Hereditary breast ovarian cancer syndromeEnrichmentATM, TP533.35
27Autoimmune lymphoproliferative syndrome, type iiaEnrichmentCASP103.23
28Intellectual developmental disorder, autosomal recessive 34, with variant lissencephalyEnrichmentCRADD3.23
29Endometrial serous adenocarcinomaEnrichmentATM3.23
30Intellectual developmental disorder, autosomal recessive 80, with variant lissencephalyEnrichmentCASP23.23
31B-cell non-hodgkin lymphomaEnrichmentATM3.23
32Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephalyEnrichmentPIDD13.23
33Adrenocortical carcinoma, hereditaryEnrichmentTP533.13
34Cervical cancerEnrichmentTP533.13
35Lymphoma, hodgkin, classicEnrichmentTP533.13
36Congenital fibrosarcomaEnrichmentTP533.13
37Li-fraumeni syndrome 1EnrichmentTP533.13
38SarcomaEnrichmentTP533.13
39Cervix carcinomaEnrichmentTP533.13
40Hodgkin's lymphomaEnrichmentTP533.13
41Pleomorphic rhabdomyosarcomaEnrichmentTP533.13
42Olmsted syndrome 2EnrichmentPERP3.13
43Erythrokeratodermia variabilis et progressiva 7EnrichmentPERP3.13
44Breast cancerEnrichmentATM, TP533.08
45Menke-hennekam syndrome 1EnrichmentCREBBP2.99
46Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.99
47Menke-hennekam syndromeEnrichmentCREBBP2.99
48Osteogenic sarcomaEnrichmentTP532.96
49Nasopharyngeal carcinomaEnrichmentTP532.96
50Atypical teratoid rhabdoid tumorEnrichmentTP532.96
51Anaplastic astrocytomaEnrichmentTP532.96
52Squamous cell carcinomaEnrichmentTP532.96
53Bone osteosarcomaEnrichmentTP532.96
54Colorectal cancerEnrichmentATM, TP532.95
55Cardiac valvular dysplasia, x-linkedEnrichmentATM2.93
56High grade gliomaEnrichmentATM2.93
57T-cell prolymphocytic leukemiaEnrichmentATM2.93
58Small cell cancer of the lungEnrichmentTP532.83
59Thyroid cancer, nonmedullary, 1EnrichmentTP532.83
60Lung sarcomatoid carcinomaEnrichmentTP532.83
61Embryonal rhabdomyosarcomaEnrichmentTP532.83
62Charcot-marie-tooth disease, demyelinating, type 4dEnrichmentNDRG12.83
63Intravascular large b-cell lymphomaEnrichmentBCL62.83
64Charcot-marie-tooth disease type 4dEnrichmentNDRG12.83
65Primary mediastinal large b-cell lymphomaEnrichmentBCL62.83
66Ovarian cancerEnrichmentATM, TP532.83
67Ataxia-telangiectasiaEnrichmentATM2.75
68Polycythemia veraEnrichmentATM2.75
69Koolen-de vries syndromeEnrichmentATM2.75
70Rhabdomyosarcoma 2EnrichmentTP532.73
71LymphomaEnrichmentTP532.73
72Acute megakaryocytic leukemiaEnrichmentTP532.73
73Thumb deformityEnrichmentCREBBP2.69
74Anemia, hypochromic microcytic, with iron overload 2EnrichmentSTEAP32.69
75Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.69
76Li-fraumeni syndromeEnrichmentTP532.66
77Adrenocortical carcinomaEnrichmentTP532.66
78Breast adenocarcinomaEnrichmentTP532.66
79High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL62.66
80Mutilating palmoplantar keratoderma with periorificial keratotic plaquesEnrichmentPERP2.66
81Autoimmune lymphoproliferative syndromeEnrichmentCASP102.63
82Mantle cell lymphomaEnrichmentATM2.63
83Oculomotor apraxiaEnrichmentATM2.63
84Inherited cancer-predisposing syndromeEnrichmentATM, TP532.60
85Esophageal cancerEnrichmentTP532.59
86Squamous cell carcinoma, head and neckEnrichmentTP532.59
87Essential thrombocythemiaEnrichmentTP532.59
88Gallbladder cancerEnrichmentTP532.59
89B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP532.59
90GlioblastomaEnrichmentATM2.53
91Glioma susceptibility 1EnrichmentTP532.53
92ChoroideremiaEnrichmentCHM2.53
93Tethered spinal cord syndromeEnrichmentCREBBP2.51
94Intraocular pressure quantitative trait locusEnrichmentCREBBP2.51
95Adult hepatocellular carcinomaEnrichmentTP532.48
96Primary hyperaldosteronismEnrichmentTP532.48
97Clear cell renal cell carcinomaEnrichmentATM2.45
98Autoinflammatory diseaseEnrichmentNLRC42.45
99Follicular lymphomaEnrichmentBCL62.43
100Night blindnessEnrichmentCHM2.43
101Familial colorectal cancerEnrichmentTP532.43
102Myelodysplastic syndromeEnrichmentTP532.39
103Renal cell carcinoma, papillary, 1EnrichmentATM2.38
104Lip and oral cavity carcinomaEnrichmentTP532.35
105Lung cancer susceptibility 3EnrichmentTP532.29
106Colonic benign neoplasmEnrichmentATM2.28
107Familial isolated arrhythmogenic right ventricular dysplasiaEnrichmentCRADD2.28
108Lynch syndrome 1EnrichmentATM2.23
109RhabdomyosarcomaEnrichmentTP532.23
110Rubinstein-taybi syndrome 1EnrichmentCREBBP2.21
111Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP2.21
112HypertrichosisEnrichmentCREBBP2.21
113Immune deficiency diseaseEnrichmentATM2.19
114Uterine corpus cancerEnrichmentATM2.19
115Familial colorectal cancer type xEnrichmentATM2.19
116Breast-ovarian cancer, familial 1EnrichmentATM2.12
117HepatoblastomaEnrichmentTP532.11
118Hepatocellular carcinomaEnrichmentTP532.09
119Diamond-blackfan anemia 1EnrichmentTP532.07
120Renal cell carcinoma, nonpapillaryEnrichmentATM2.05
121Endometrial cancerEnrichmentATM1.91
122Charcot-marie-tooth disease type 4EnrichmentNDRG11.88
123Diamond-blackfan anemiaEnrichmentTP531.88
124Heart diseaseEnrichmentCREBBP1.84
125Leukemia, acute myeloidEnrichmentTP531.83
126Corpus callosum, agenesis ofEnrichmentCREBBP1.81
127Isolated corpus callosum agenesisEnrichmentCREBBP1.81
128Rare genetic intellectual disabilityEnrichmentCREBBP1.81
129Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.81
130Severe covid-19EnrichmentCASP101.77
131ScoliosisEnrichmentCREBBP1.61
132Eye diseaseEnrichmentCHM1.59
133Charcot-marie-tooth diseaseEnrichmentNDRG11.53
134Autosomal recessive non-syndromic intellectual disabilityEnrichmentCRADD1.47
135AutismEnrichmentCREBBP1.14
136Congenital nervous system abnormalityEnrichmentCREBBP0.98
137Nervous system diseaseEnrichmentCREBBP0.98
138Retinitis pigmentosaEnrichmentCHM0.84
139Hereditary retinal dystrophyEnrichmentCHM0.71
140Fundus dystrophyEnrichmentCHM0.71

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