miRNA regulation of p53 pathway in prostate cancer

No Pathway Network information available for miRNA regulation of p53 pathway in prostate cancer

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

Disorders associated with miRNA regulation of p53 pathway in prostate cancer SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Li-fraumeni syndromeEnrichmentCHEK2, MDM2, TP536.62
2Squamous cell carcinoma, head and neckEnrichmentPTEN, TNFRSF10B, TP536.38
3Prostate cancerEnrichmentATM, CHEK2, PTEN, TP536.24
4Breast cancerEnrichmentATM, CASP8, CHEK2, PTEN, TP536.09
5Uterine corpus cancerEnrichmentATM, CHEK2, PTEN5.71
6Gastric cancerEnrichmentATM, CHEK2, PTEN, TP535.53
7Hereditary breast carcinomaEnrichmentATM, CHEK2, PTEN, TP535.49
8Li-fraumeni syndrome 1EnrichmentCHEK2, TP535.27
9SarcomaEnrichmentCHEK2, TP535.27
10Hereditary breast ovarian cancer syndromeEnrichmentATM, CHEK2, PTEN, TP535.10
11Diffuse large b-cell lymphomaEnrichmentCHEK2, PTEN, TP534.95
12Endometrial cancerEnrichmentATM, CHEK2, PTEN4.81
13Osteogenic sarcomaEnrichmentCHEK2, TP534.79
14AdenocarcinomaEnrichmentATM, TP534.79
15Laryngeal squamous cell carcinomaEnrichmentPTEN, TNFRSF10B4.79
16Bone osteosarcomaEnrichmentCHEK2, TP534.79
17Pancreatic cancerEnrichmentATM, CHEK2, TP534.58
18Bladder cancerEnrichmentATM, PTEN, TP534.38
19Colorectal cancerEnrichmentATM, BAX, CHEK2, TP534.31
20Acute megakaryocytic leukemiaEnrichmentPTEN, TP534.27
21Ovarian cancerEnrichmentATM, CHEK2, PTEN, TP534.05
22Adult hepatocellular carcinomaEnrichmentCASP8, TP533.72
23Colonic benign neoplasmEnrichmentATM, CHEK23.72
24Lynch syndrome 1EnrichmentATM, CHEK23.62
25Leukemia, chronic lymphocyticEnrichmentATM, TP533.62
26MelanomaEnrichmentCHEK2, PTEN3.62
27Inherited cancer-predisposing syndromeEnrichmentATM, CHEK2, PTEN, TP533.60
28Familial colorectal cancer type xEnrichmentATM, CHEK23.53
29Breast-ovarian cancer, familial 1EnrichmentATM, CHEK23.38
30RhabdomyosarcomaEnrichmentPTEN, TP533.20
31GliosarcomaEnrichmentATM, TP533.20
32Giant cell glioblastomaEnrichmentATM, TP533.14
33Hepatocellular carcinomaEnrichmentCASP8, TP532.92
34Vacterl association with hydrocephalusEnrichmentPTEN2.63
35Caspase 8 deficiencyEnrichmentCASP82.63
36Accelerated tumor formationEnrichmentMDM22.63
37Lessel-kubisch syndromeEnrichmentMDM22.63
38Bone marrow failure syndrome 5EnrichmentTP532.63
39Papilloma of choroid plexusEnrichmentTP532.63
40Basal cell carcinoma 7EnrichmentTP532.63
41Anaplastic thyroid carcinomaEnrichmentTP532.63
42Plasminogen activator inhibitor-1 deficiencyEnrichmentSERPINE12.63
43Papillary tumor of the pineal regionEnrichmentPTEN2.63
44Tumor predisposition syndrome 4EnrichmentCHEK22.63
45Olmsted syndrome 2EnrichmentPERP2.63
46Endometrial serous adenocarcinomaEnrichmentATM2.63
47Glioma susceptibility 2EnrichmentPTEN2.63
48Ductal carcinoma in situEnrichmentTP532.63
49LeiomyosarcomaEnrichmentCHEK22.63
50Erythrokeratodermia variabilis et progressiva 7EnrichmentPERP2.63
51Thyroid gland undifferentiated carcinomaEnrichmentTP532.63
52Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.63
53Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.63
54B-cell non-hodgkin lymphomaEnrichmentATM2.63
55Choroid plexus cancerEnrichmentTP532.63
56Pleomorphic xanthoastrocytomaEnrichmentTP532.63
57Congenital plasminogen activator inhibitor type 1 deficiencyEnrichmentSERPINE12.63
58Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeEnrichmentPTEN2.63
59Lung cancerEnrichmentCASP8, CHEK22.59
60Adrenocortical carcinoma, hereditaryEnrichmentTP532.33
61Cervical cancerEnrichmentTP532.33
62Xeroderma pigmentosum, complementation group eEnrichmentDDB22.33
63Lymphoma, hodgkin, classicEnrichmentTP532.33
64Congenital heart defects, multiple types, 3EnrichmentCHEK22.33
65Cardiac valvular dysplasia, x-linkedEnrichmentATM2.33
66Congenital fibrosarcomaEnrichmentTP532.33
67High grade gliomaEnrichmentATM2.33
68Cervix carcinomaEnrichmentTP532.33
69Hodgkin's lymphomaEnrichmentTP532.33
70T-cell prolymphocytic leukemiaEnrichmentATM2.33
71Buratti-harel syndromeEnrichmentSIAH12.33
72Vacterl with hydrocephalusEnrichmentPTEN2.33
73Juvenile polyposis of infancyEnrichmentPTEN2.33
74Xeroderma pigmentosum group eEnrichmentDDB22.33
75Pleomorphic rhabdomyosarcomaEnrichmentTP532.33
76Ataxia-telangiectasiaEnrichmentATM2.15
77Polycythemia veraEnrichmentATM2.15
78Nasopharyngeal carcinomaEnrichmentTP532.15
79Koolen-de vries syndromeEnrichmentATM2.15
80Dedifferentiated liposarcomaEnrichmentMDM22.15
81Mutilating palmoplantar keratoderma with periorificial keratotic plaquesEnrichmentPERP2.15
82Atypical teratoid rhabdoid tumorEnrichmentTP532.15
83Anaplastic astrocytomaEnrichmentTP532.15
84Squamous cell carcinomaEnrichmentTP532.15
85T-cell acute lymphoblastic leukemiaEnrichmentBAX2.15
86Well-differentiated liposarcomaEnrichmentMDM22.15
87Myeloma, multipleEnrichmentATM, TP532.12
88Small cell cancer of the lungEnrichmentTP532.03
89Thyroid cancer, nonmedullary, 1EnrichmentTP532.03
90Mantle cell lymphomaEnrichmentATM2.03
91Lung sarcomatoid carcinomaEnrichmentTP532.03
92Embryonal rhabdomyosarcomaEnrichmentTP532.03
93Hemoglobin c diseaseEnrichmentCHEK22.03
94GliomaEnrichmentPTEN2.03
95Oculomotor apraxiaEnrichmentATM2.03
96Pseudomyogenic hemangioendotheliomaEnrichmentSERPINE12.03
97Rhabdomyosarcoma 2EnrichmentTP531.93
98Macrocephaly/autism syndromeEnrichmentPTEN1.93
99LymphomaEnrichmentTP531.93
100GlioblastomaEnrichmentATM1.93
101HemangiomaEnrichmentPTEN1.93
102HemimegalencephalyEnrichmentPTEN1.93
103Cowden syndrome 1EnrichmentPTEN1.85
104Wilms tumor 5EnrichmentCHEK21.85
105Adrenocortical carcinomaEnrichmentTP531.85
106Clear cell renal cell carcinomaEnrichmentATM1.85
107Breast adenocarcinomaEnrichmentTP531.85
108Esophageal cancerEnrichmentTP531.79
109Thyroid cancer, nonmedullary, 2EnrichmentPTEN1.79
110Renal cell carcinoma, papillary, 1EnrichmentATM1.79
111Essential thrombocythemiaEnrichmentTP531.79
112Gallbladder cancerEnrichmentTP531.79
113Follicular thyroid carcinomaEnrichmentPTEN1.79
114B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.79
115Glioma susceptibility 1EnrichmentTP531.73
116Polycystic kidney disease 4 with or without polycystic liver diseaseEnrichmentCYS11.73
117Lymphoma, non-hodgkin, familialEnrichmentTP531.73
118Primary hyperaldosteronismEnrichmentTP531.68
119Cowden syndromeEnrichmentPTEN1.68
120Familial colorectal cancerEnrichmentTP531.63
121Immune deficiency diseaseEnrichmentATM1.59
122Xeroderma pigmentosum, variant typeEnrichmentDDB21.59
123Meningioma, familialEnrichmentPTEN1.59
124Myelodysplastic syndromeEnrichmentTP531.59
125MeningiomaEnrichmentPTEN1.55
126Lip and oral cavity carcinomaEnrichmentTP531.55
127Nk-cell enteropathyEnrichmentCHEK21.52
128Lung cancer susceptibility 3EnrichmentTP531.49
129Renal cell carcinoma, nonpapillaryEnrichmentATM1.46
130Wilms tumor 1EnrichmentCHEK21.46
131Lynch syndromeEnrichmentCHEK21.46
132HepatoblastomaEnrichmentTP531.31
133Diamond-blackfan anemia 1EnrichmentTP531.28
134Diamond-blackfan anemiaEnrichmentTP531.09
135Leukemia, acute myeloidEnrichmentTP531.04
136Primary ovarian insufficiencyEnrichmentCHEK20.88
137Congenital nervous system abnormalityEnrichmentPTEN0.65
138Nervous system diseaseEnrichmentPTEN0.65
139Autism spectrum disorderEnrichmentPTEN0.64
140Complex neurodevelopmental disorderEnrichmentSIAH10.59

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