p53 Signaling

No Pathway Network information available for p53 Signaling

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

Disorders associated with p53 Signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Gastric cancerEnrichmentBRCA1, CASP10, CDK4, CHEK2, PTEN, TP537.42
2Bladder cancerEnrichmentATM, BRCA1, CDKN1A, PTEN, RB1, TP537.07
3Osteogenic sarcomaEnrichmentCHEK2, RB1, TP537.04
4Bone osteosarcomaEnrichmentCHEK2, RB1, TP537.04
5Lung cancerEnrichmentBRCA1, CASP8, CHEK2, FAS, FASLG6.51
6Autoimmune lymphoproliferative syndromeEnrichmentCASP10, FAS, FASLG6.44
7Colorectal cancerEnrichmentAKT1, ATM, BAX, BRCA1, CCND1, CHEK2, EP300, TP536.40
8Breast cancerEnrichmentAKT1, BRCA1, CASP8, CHEK2, PTEN, TP535.95
9Uterine corpus cancerEnrichmentATM, BRCA1, CHEK2, PTEN5.94
10Hereditary breast carcinomaEnrichmentAKT1, ATM, BRCA1, CHEK2, PTEN, TP535.94
11Li-fraumeni syndromeEnrichmentCHEK2, MDM2, TP535.74
12Prostate cancerEnrichmentATM, BRCA1, CHEK2, PTEN, TP535.55
13Squamous cell carcinoma, head and neckEnrichmentPTEN, TNFRSF10B, TP535.50
14Ovarian cancerEnrichmentAKT1, BRCA1, CHEK2, PTEN, RB1, TP535.19
15Endometrial cancerEnrichmentATM, BRCA1, CHEK2, PTEN4.70
16Li-fraumeni syndrome 1EnrichmentCHEK2, TP534.69
17SarcomaEnrichmentCHEK2, TP534.69
18Inherited cancer-predisposing syndromeEnrichmentBRCA1, CDK4, CHEK2, PTEN, RB1, TP534.53
19Pancreatic cancerEnrichmentATM, BRCA1, CHEK2, TP534.39
20RhabdomyosarcomaEnrichmentBRCA1, PTEN, TP534.31
21Leukemia, chronic lymphocyticEnrichmentATM, CCND1, TP534.26
22Dedifferentiated liposarcomaEnrichmentCDK4, MDM24.21
23Squamous cell carcinomaEnrichmentRB1, TP534.21
24Laryngeal squamous cell carcinomaEnrichmentPTEN, TNFRSF10B4.21
25Well-differentiated liposarcomaEnrichmentCDK4, MDM24.21
26Hereditary breast ovarian cancer syndromeEnrichmentATM, BRCA1, CHEK2, PTEN, TP534.15
27Diffuse large b-cell lymphomaEnrichmentCHEK2, PTEN, TP534.08
28Lip and oral cavity carcinomaEnrichmentABL1, RB1, TP534.00
29Small cell cancer of the lungEnrichmentRB1, TP533.91
30Breast-ovarian cancer, familial 1EnrichmentATM, BRCA1, CHEK23.89
31T-cell acute lymphoblastic leukemiaEnrichmentABL1, BAX3.74
32AdenocarcinomaEnrichmentATM, TP533.74
33Acute megakaryocytic leukemiaEnrichmentPTEN, TP533.69
34HemimegalencephalyEnrichmentAKT3, PTEN3.69
35Breast adenocarcinomaEnrichmentAKT1, TP533.52
36Mantle cell lymphomaEnrichmentATM, CCND13.44
37Lymphoma, non-hodgkin, familialEnrichmentCASP10, TP533.25
38Adult hepatocellular carcinomaEnrichmentCASP8, TP533.14
39Cowden syndromeEnrichmentAKT1, PTEN3.14
40MelanomaEnrichmentCHEK2, PTEN3.04
41B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentABL1, TP532.90
42MeningiomaEnrichmentAKT1, PTEN2.88
43Lung cancer susceptibility 3EnrichmentRB1, TP532.74
44Colonic benign neoplasmEnrichmentATM, CHEK22.67
45Lynch syndrome 1EnrichmentATM, CHEK22.57
46PolymicrogyriaEnrichmentAKT3, PSMC32.57
47Familial colorectal cancer type xEnrichmentATM, CHEK22.49
48Hepatocellular carcinomaEnrichmentCASP8, TP532.35
49Palmoplantar keratoderma, punctate type iiEnrichmentBRCA12.34
50Proteus syndromeEnrichmentAKT12.34
51Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.34
52Vacterl association with hydrocephalusEnrichmentPTEN2.34
53Caspase 8 deficiencyEnrichmentCASP82.34
54Melanoma, cutaneous malignant 3EnrichmentCDK42.34
55Accelerated tumor formationEnrichmentMDM22.34
56Ichthyosis, congenital, autosomal recessive 12EnrichmentCASP142.34
57Noonan syndrome 13EnrichmentMAPK12.34
58Chromosome 2q37 deletion syndromeEnrichmentHDAC42.34
59Lessel-kubisch syndromeEnrichmentMDM22.34
60Cornelia de lange syndrome 5EnrichmentHDAC82.34
61Bone marrow failure syndrome 5EnrichmentTP532.34
62Papilloma of choroid plexusEnrichmentTP532.34
63Basal cell carcinoma 7EnrichmentTP532.34
64Anaplastic thyroid carcinomaEnrichmentTP532.34
65Infant-type hemispheric gliomaEnrichmentBRCA12.34
66Papillary tumor of the pineal regionEnrichmentPTEN2.34
67Tumor predisposition syndrome 4EnrichmentCHEK22.34
68Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.34
69Autoimmune lymphoproliferative syndrome, type iiaEnrichmentCASP102.34
70Cowden syndrome 6EnrichmentAKT12.34
71Glioma susceptibility 2EnrichmentPTEN2.34
72Ductal carcinoma in situEnrichmentTP532.34
73Neurodevelopmental disorder with central hypotonia and dysmorphic faciesEnrichmentHDAC42.34
74LeiomyosarcomaEnrichmentCHEK22.34
75Thyroid gland undifferentiated carcinomaEnrichmentTP532.34
76Trilateral retinoblastomaEnrichmentRB12.34
77Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.34
78Intellectual developmental disorder, autosomal recessive 80, with variant lissencephalyEnrichmentCASP22.34
79Capillary hemangiomaEnrichmentAKT32.34
80Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.34
81Oocyte/zygote/embryo maturation arrest 21EnrichmentCHEK12.34
82Choroid plexus cancerEnrichmentTP532.34
83Pleomorphic xanthoastrocytomaEnrichmentTP532.34
84Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeEnrichmentPTEN2.34
85Lethal brain and heart developmental defectsEnrichmentSIRT62.34
86Primary peritoneal carcinomaEnrichmentBRCA12.34
87Akt2-related familial partial lipodystrophyEnrichmentAKT22.34
88Lung oat cell carcinomaEnrichmentRB12.34
89GliosarcomaEnrichmentATM, TP532.16
90Giant cell glioblastomaEnrichmentATM, TP532.11
91Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmiaEnrichmentHDAC62.10
92Seckel syndrome 1EnrichmentATR2.10
93Advanced sleep phase syndrome, familial, 2EnrichmentCSNK1D2.10
94Neurodevelopmental disorder with microcephaly, hypotonia, and absent languageEnrichmentPSMB12.10
95Auriculocondylar syndrome 4EnrichmentHDAC92.10
96Deafness, cataract, impaired intellectual development, and polyneuropathyEnrichmentPSMC32.10
97Cutaneous telangiectasia and cancer syndrome, familialEnrichmentATR2.10
98Immunodeficiency 26 with or without neurologic abnormalitiesEnrichmentPRKDC2.10
99Endometrial serous adenocarcinomaEnrichmentATM2.10
100B-cell non-hodgkin lymphomaEnrichmentATM2.10
101Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndromeEnrichmentATR2.10
102Scoliosis, isolated 1EnrichmentMAPK72.04
103Adrenocortical carcinoma, hereditaryEnrichmentTP532.04
104Cervical cancerEnrichmentTP532.04
105Chromosome 13q14 deletion syndromeEnrichmentRB12.04
106Lymphoma, hodgkin, classicEnrichmentTP532.04
107Syndactyly, type iiiEnrichmentHDAC82.04
108Congenital heart defects, multiple types, 3EnrichmentCHEK22.04
109Fanconi anemia, complementation group sEnrichmentBRCA12.04
110Intravascular large b-cell lymphomaEnrichmentBCL22.04
111Pancreatic cancer 4EnrichmentBRCA12.04
112Wilson-turner syndromeEnrichmentHDAC82.04
113Senior-loken syndrome 7EnrichmentAKT32.04
114Congenital fibrosarcomaEnrichmentTP532.04
115Cervix carcinomaEnrichmentTP532.04
116Hodgkin's lymphomaEnrichmentTP532.04
117Bardet-biedl syndrome 16EnrichmentAKT32.04
118Inflammatory breast carcinomaEnrichmentBRCA12.04
119Peritoneum cancerEnrichmentBRCA12.04
120Bilateral breast cancerEnrichmentBRCA12.04
121Vacterl with hydrocephalusEnrichmentPTEN2.04
122Familial retinoblastomaEnrichmentRB12.04
123Juvenile polyposis of infancyEnrichmentPTEN2.04
124Pleomorphic rhabdomyosarcomaEnrichmentTP532.04
125Myeloma, multipleEnrichmentATM, CCND1, TP532.01
126Primary ovarian insufficiencyEnrichmentCHEK2, SIRT6, THBS11.95
127RetinoblastomaEnrichmentRB11.86
128Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG1.86
129Nasopharyngeal carcinomaEnrichmentTP531.86
130Woolly hair, autosomal recessive 3EnrichmentRB11.86
131Hypotrichosis 8EnrichmentRB11.86
132Renu syndromeEnrichmentSIRT41.86
133High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL21.86
134Atypical teratoid rhabdoid tumorEnrichmentTP531.86
135Anaplastic astrocytomaEnrichmentTP531.86
136EnchondromatosisEnrichmentHIF1A1.86
137Vogt-koyanagi-harada diseaseEnrichmentFAS1.86
138Congenital heart defects and skeletal malformations syndromeEnrichmentABL11.80
139Birk-aharoni syndromeEnrichmentPSMC11.80
140Cardiac valvular dysplasia, x-linkedEnrichmentATM1.80
141Menke-hennekam syndrome 2EnrichmentEP3001.80
142Proteasome-associated autoinflammatory syndrome 3EnrichmentPSMB41.80
143High grade gliomaEnrichmentATM1.80
144T-cell prolymphocytic leukemiaEnrichmentATM1.80
145Submucosal cleft palateEnrichmentUBB1.80
146Cleft hard palateEnrichmentUBB1.80
147MicrocephalyEnrichmentABL1, EP300, HDAC8, PSMC31.79
148Thyroid cancer, nonmedullary, 1EnrichmentTP531.74
149Polyposis syndrome, hereditary mixed, 1EnrichmentBRCA11.74
150Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT31.74
151Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.74
152Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT31.74
153CholangiocarcinomaEnrichmentBRCA11.74
154Lynch syndrome 4EnrichmentRB11.74
155Congenital generalized lipodystrophyEnrichmentFOS1.74
156Lung sarcomatoid carcinomaEnrichmentTP531.74
157Embryonal rhabdomyosarcomaEnrichmentTP531.74
158Hemoglobin c diseaseEnrichmentCHEK21.74
159GliomaEnrichmentPTEN1.74
160Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentCHEK11.74
161Enchondromatosis, multiple, ollier typeEnrichmentHIF1A1.64
162Rhabdomyosarcoma 2EnrichmentTP531.64
163Macrocephaly/autism syndromeEnrichmentPTEN1.64
164Breast-ovarian cancer, familial 2EnrichmentBRCA11.64
165Follicular lymphomaEnrichmentBCL21.64
166LymphomaEnrichmentTP531.64
167HemangiomaEnrichmentPTEN1.64
168Histiocytoid hemangiomaEnrichmentFOS1.64
169Ataxia-telangiectasiaEnrichmentATM1.63
170Proteasome-associated autoinflammatory syndrome 1EnrichmentPSMB41.63
171Polycythemia veraEnrichmentATM1.63
172Uvula, bifidEnrichmentUBB1.63
173Cleft soft palateEnrichmentUBB1.63
174Koolen-de vries syndromeEnrichmentATM1.63
175Proteosome-associated autoinflammatory syndromeEnrichmentPSMB41.63
176Advanced sleep phase syndromeEnrichmentCSNK1D1.63
177Thyroid hemiagenesisEnrichmentPSMD31.63
178Cowden syndrome 1EnrichmentPTEN1.57
179Wilms tumor 5EnrichmentCHEK21.57
180Adrenocortical carcinomaEnrichmentTP531.57
181Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentABL11.51
182Oculomotor apraxiaEnrichmentATM1.51
183Esophageal cancerEnrichmentTP531.50
184Multiple endocrine neoplasia, type iEnrichmentCDKN1A1.50
185Thyroid cancer, nonmedullary, 2EnrichmentPTEN1.50
186Multiple enchondromatosis, maffucci typeEnrichmentHIF1A1.50
187Essential thrombocythemiaEnrichmentTP531.50
188Gallbladder cancerEnrichmentTP531.50
189MegacolonEnrichmentAKT31.50
190Follicular thyroid carcinomaEnrichmentPTEN1.50
191Glioma susceptibility 1EnrichmentTP531.44
192Fanconi anemia, complementation group cEnrichmentHDAC81.44
193Von hippel-lindau syndromeEnrichmentCCND11.41
194Rubinstein-taybi syndrome 2EnrichmentEP3001.41
195GlioblastomaEnrichmentATM1.41
196Cornelia de lange syndrome 1EnrichmentHDAC81.39
197Primary hyperaldosteronismEnrichmentTP531.39
198Cornelia de lange syndromeEnrichmentHDAC81.39
199Familial colorectal cancerEnrichmentTP531.35
200Developmental dysplasia of the hip 1EnrichmentPSMC31.33
201Rubinstein-taybi syndrome 1EnrichmentEP3001.33
202Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.33
203Patent ductus arteriosusEnrichmentPSMC31.33
204Clear cell renal cell carcinomaEnrichmentATM1.33
205Meningioma, familialEnrichmentPTEN1.31
206Myelodysplastic syndromeEnrichmentTP531.31
207Atrial heart septal defectEnrichmentHDAC81.31
208Interatrial communicationEnrichmentHDAC81.31
209Specific learning disabilityEnrichmentMAPK11.31
210Leukemia, chronic myeloidEnrichmentABL11.27
211Renal cell carcinoma, papillary, 1EnrichmentATM1.27
212Moyamoya angiopathyEnrichmentABL11.27
213Nk-cell enteropathyEnrichmentCHEK21.24
214Lennox-gastaut syndromeEnrichmentMAPK101.21
215Periventricular nodular heterotopiaEnrichmentBRCA11.21
216Wilms tumor 1EnrichmentCHEK21.18
217Lynch syndromeEnrichmentCHEK21.18
218Charge syndromeEnrichmentEP3001.16
219Melanoma, cutaneous malignant 1EnrichmentCDK41.13
220Heart, malformation ofEnrichmentMAPK11.10
221Polycystic kidney diseaseEnrichmentHDAC81.10
222Behcet syndromeEnrichmentFAS1.08
223Immune deficiency diseaseEnrichmentATM1.08
224HepatoblastomaEnrichmentTP531.04
225Acute promyelocytic leukemiaEnrichmentPML1.01
226Diamond-blackfan anemia 1EnrichmentTP531.00
227Seckel syndromeEnrichmentATR0.98
228Heart diseaseEnrichmentABL10.98
229Renal cell carcinoma, nonpapillaryEnrichmentATM0.95
230Polydactyly, postaxial, type a1EnrichmentEP3000.95
231Rare genetic intellectual disabilityEnrichmentEP3000.95
232Severe covid-19EnrichmentCASP100.90
233Patent foramen ovaleEnrichmentPSMC30.88
234NephronophthisisEnrichmentPIAS10.85
235Fanconi anemia, complementation group aEnrichmentBRCA10.83
236Diamond-blackfan anemiaEnrichmentTP530.82
237Myocardial infarctionEnrichmentPSMA60.80
238Precursor t-cell acute lymphoblastic leukemiaEnrichmentABL10.78
239Leukemia, acute myeloidEnrichmentTP530.78
240Type 2 diabetes mellitusEnrichmentAKT20.76
241Congenital nervous system abnormalityEnrichmentPTEN0.41
242Nervous system diseaseEnrichmentPTEN0.41
243Autism spectrum disorderEnrichmentPTEN0.40

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