miRNA regulation of DNA damage response

No Pathway Network information available for miRNA regulation of DNA damage response

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

Disorders associated with miRNA regulation of DNA damage response SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Breast cancerEnrichmentAKT1, ATM, BRCA1, CASP8, CHEK2, MRE11, NBN, RAD50, RAD51, TP5316.00
2Ovarian cancerEnrichmentAKT1, ATM, BRCA1, CDKN1B, CHEK2, FANCD2, MRE11, NBN, RAD50, RB1, TP5316.00
3Hereditary breast carcinomaEnrichmentAKT1, ATM, BRCA1, CHEK2, NBN, RAD50, RAD51, TP5310.58
4Hereditary breast ovarian cancer syndromeEnrichmentATM, BRCA1, CHEK2, MRE11, NBN, RAD50, RAD51, TP539.52
5Inherited cancer-predisposing syndromeEnrichmentATM, BRCA1, CDK4, CDKN1B, CHEK2, MRE11, NBN, RAD50, RB1, TP538.95
6Gastric cancerEnrichmentATM, BRCA1, CDK4, CHEK2, NBN, TP537.14
7Osteogenic sarcomaEnrichmentCHEK2, RB1, TP536.90
8Bone osteosarcomaEnrichmentCHEK2, RB1, TP536.90
9Pancreatic cancerEnrichmentATM, BRCA1, CHEK2, NBN, TP536.84
10Colorectal cancerEnrichmentAKT1, ATM, BAX, BRCA1, CCND1, CHEK2, TP536.56
11Bladder cancerEnrichmentATM, BRCA1, CDKN1A, RB1, TP536.50
12Prostate cancerEnrichmentATM, BRCA1, CHEK2, NBN, TP536.50
13Breast-ovarian cancer, familial 1EnrichmentATM, BRCA1, CHEK2, NBN6.37
14Li-fraumeni syndromeEnrichmentCHEK2, MDM2, TP535.60
15Hepatocellular carcinomaEnrichmentCASP8, NBN, RAD50, TP535.38
16Colonic benign neoplasmEnrichmentATM, CHEK2, MRE114.98
17Leukemia, chronic lymphocyticEnrichmentATM, CCND1, TP534.83
18Lung cancerEnrichmentBRCA1, CASP8, CHEK2, FAS4.70
19Uterine corpus cancerEnrichmentATM, BRCA1, CHEK24.69
20Li-fraumeni syndrome 1EnrichmentCHEK2, TP534.59
21SarcomaEnrichmentCHEK2, TP534.59
22Lip and oral cavity carcinomaEnrichmentABL1, RB1, TP534.57
23Dedifferentiated liposarcomaEnrichmentCDK4, MDM24.12
24Squamous cell carcinomaEnrichmentRB1, TP534.12
25T-cell acute lymphoblastic leukemiaEnrichmentABL1, BAX4.12
26AdenocarcinomaEnrichmentATM, TP534.12
27Well-differentiated liposarcomaEnrichmentCDK4, MDM24.12
28Diffuse large b-cell lymphomaEnrichmentCHEK2, NBN, TP533.94
29Small cell cancer of the lungEnrichmentRB1, TP533.82
30Mantle cell lymphomaEnrichmentATM, CCND13.82
31Nijmegen breakage syndrome-like disorderEnrichmentMRE11, RAD503.82
32Endometrial cancerEnrichmentATM, BRCA1, CHEK23.80
33Von hippel-lindau syndromeEnrichmentCCND1, FANCD23.60
34Breast adenocarcinomaEnrichmentAKT1, TP533.42
35Multiple endocrine neoplasia, type iEnrichmentCDKN1A, CDKN1B3.28
36Squamous cell carcinoma, head and neckEnrichmentTNFRSF10B, TP533.28
37B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentABL1, TP533.28
38Fanconi anemia, complementation group aEnrichmentBRCA1, FANCD2, RAD513.13
39Adult hepatocellular carcinomaEnrichmentCASP8, TP533.05
40Lynch syndrome 1EnrichmentATM, CHEK22.95
41Familial colorectal cancer type xEnrichmentATM, CHEK22.87
42Lung cancer susceptibility 3EnrichmentRB1, TP532.65
43Seckel syndromeEnrichmentATR, ATRIP2.65
44Myeloma, multipleEnrichmentATM, CCND1, TP532.54
45RhabdomyosarcomaEnrichmentBRCA1, TP532.53
46GliosarcomaEnrichmentATM, TP532.53
47Giant cell glioblastomaEnrichmentATM, TP532.48
48Palmoplantar keratoderma, punctate type iiEnrichmentBRCA12.29
49Proteus syndromeEnrichmentAKT12.29
50Developmental and epileptic encephalopathy 85 with or without midline brain defectsEnrichmentSMC1A2.29
51Caspase 8 deficiencyEnrichmentCASP82.29
52Melanoma, cutaneous malignant 3EnrichmentCDK42.29
53Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3EnrichmentCCND22.29
54Seckel syndrome 1EnrichmentATR2.29
55Microcephaly 12, primary, autosomal recessiveEnrichmentCDK62.29
56Mirror movements 2EnrichmentRAD512.29
57Accelerated tumor formationEnrichmentMDM22.29
58Lissencephaly 7 with cerebellar hypoplasiaEnrichmentCDK52.29
59Fanconi anemia, complementation group rEnrichmentRAD512.29
60Lessel-kubisch syndromeEnrichmentMDM22.29
61Bone marrow failure syndrome 5EnrichmentTP532.29
62Papilloma of choroid plexusEnrichmentTP532.29
63Basal cell carcinoma 7EnrichmentTP532.29
64Anaplastic thyroid carcinomaEnrichmentTP532.29
65Infant-type hemispheric gliomaEnrichmentBRCA12.29
66Mitochondrial dna depletion syndrome 8bEnrichmentRRM2B2.29
67Tumor predisposition syndrome 4EnrichmentCHEK22.29
68Thrombocytopenia 4EnrichmentCYCS2.29
69Ataxia-telangiectasia-like disorder 1EnrichmentMRE112.29
70Neuroendocrine tumorEnrichmentCDKN1B2.29
71Cutaneous telangiectasia and cancer syndrome, familialEnrichmentATR2.29
72Immunodeficiency 26 with or without neurologic abnormalitiesEnrichmentPRKDC2.29
73Cowden syndrome 6EnrichmentAKT12.29
74Endometrial serous adenocarcinomaEnrichmentATM2.29
75Ductal carcinoma in situEnrichmentTP532.29
76LeiomyosarcomaEnrichmentCHEK22.29
77Thyroid gland undifferentiated carcinomaEnrichmentTP532.29
78Trilateral retinoblastomaEnrichmentRB12.29
79Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.29
80Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.29
81Oocyte/zygote/embryo maturation arrest 21EnrichmentCHEK12.29
82B-cell non-hodgkin lymphomaEnrichmentATM2.29
83Choroid plexus cancerEnrichmentTP532.29
84Pleomorphic xanthoastrocytomaEnrichmentTP532.29
85Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephalyEnrichmentPIDD12.29
86Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndromeEnrichmentATR2.29
87Rrm2b mitochondrial dna maintenance defectsEnrichmentRRM2B2.29
88Primary peritoneal carcinomaEnrichmentBRCA12.29
89Lung oat cell carcinomaEnrichmentRB12.29
90Precursor t-cell acute lymphoblastic leukemiaEnrichmentABL1, MYC2.22
91Fanconi renotubular syndrome 1EnrichmentRRM2B1.99
92Burkitt lymphomaEnrichmentMYC1.99
93Adrenocortical carcinoma, hereditaryEnrichmentTP531.99
94Cervical cancerEnrichmentTP531.99
95Cornelia de lange syndrome 2EnrichmentSMC1A1.99
96Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunctionEnrichmentRRM2B1.99
97Xeroderma pigmentosum, complementation group eEnrichmentDDB21.99
98Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 5EnrichmentRRM2B1.99
99Histiocytoma, angiomatoid fibrousEnrichmentCREB11.99
100Mitochondrial dna depletion syndrome 8aEnrichmentRRM2B1.99
101Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 2EnrichmentRRM2B1.99
102Chromosome 13q14 deletion syndromeEnrichmentRB11.99
103Lymphoma, hodgkin, classicEnrichmentTP531.99
104Multiple endocrine neoplasia, type ivEnrichmentCDKN1B1.99
105Cerebellar ataxia, neuropathy, and vestibular areflexia syndromeEnrichmentRFC11.99
106Congenital heart defects, multiple types, 3EnrichmentCHEK21.99
107Congenital heart defects and skeletal malformations syndromeEnrichmentABL11.99
108Fanconi anemia, complementation group sEnrichmentBRCA11.99
109Cardiac valvular dysplasia, x-linkedEnrichmentATM1.99
110Pancreatic cancer 4EnrichmentBRCA11.99
111Congenital fibrosarcomaEnrichmentTP531.99
112High grade gliomaEnrichmentATM1.99
113Cervix carcinomaEnrichmentTP531.99
114Hodgkin's lymphomaEnrichmentTP531.99
115T-cell prolymphocytic leukemiaEnrichmentATM1.99
116Inflammatory breast carcinomaEnrichmentBRCA11.99
117Peritoneum cancerEnrichmentBRCA11.99
118Bilateral breast cancerEnrichmentBRCA11.99
119Familial retinoblastomaEnrichmentRB11.99
120Xeroderma pigmentosum group eEnrichmentDDB21.99
121Pleomorphic rhabdomyosarcomaEnrichmentTP531.99
122RetinoblastomaEnrichmentRB11.82
123Ataxia-telangiectasiaEnrichmentATM1.82
124Vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestationsEnrichmentATRIP1.82
125Nijmegen breakage syndromeEnrichmentNBN1.82
126Polycythemia veraEnrichmentATM1.82
127Chilblain lupus 1EnrichmentATRIP1.82
128Nasopharyngeal carcinomaEnrichmentTP531.82
129Woolly hair, autosomal recessive 3EnrichmentRB11.82
130Intellectual developmental disorder, autosomal dominant 57EnrichmentTLK21.82
131Hypotrichosis 8EnrichmentRB11.82
132Koolen-de vries syndromeEnrichmentATM1.82
133High-grade b-cell lymphoma double-hit/triple-hitEnrichmentMYC1.82
134Chilblain lupusEnrichmentATRIP1.82
135Atypical teratoid rhabdoid tumorEnrichmentTP531.82
136Anaplastic astrocytomaEnrichmentTP531.82
137Laryngeal squamous cell carcinomaEnrichmentTNFRSF10B1.82
138Idiopathic camptocormiaEnrichmentRRM2B1.82
139Melanoma of soft tissueEnrichmentCREB11.82
140Vogt-koyanagi-harada diseaseEnrichmentFAS1.82
141Leukemia, acute myeloidEnrichmentFANCD2, TP531.76
142Mirror movements 1EnrichmentRAD511.69
143Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemiaEnrichmentMRE111.69
144Erythrocytosis, familial, 2EnrichmentFANCD21.69
145Thyroid cancer, nonmedullary, 1EnrichmentTP531.69
146Polyposis syndrome, hereditary mixed, 1EnrichmentBRCA11.69
147Autoimmune lymphoproliferative syndromeEnrichmentFAS1.69
148Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentCCND21.69
149CholangiocarcinomaEnrichmentBRCA11.69
150Aicardi-goutieres syndrome 1EnrichmentATRIP1.69
151Lynch syndrome 4EnrichmentRB11.69
152Lung sarcomatoid carcinomaEnrichmentTP531.69
153Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentABL11.69
154Embryonal rhabdomyosarcomaEnrichmentTP531.69
155Pregnancy loss, recurrent 1EnrichmentCCNB31.69
156Hemoglobin c diseaseEnrichmentCHEK21.69
157Primary hyperparathyroidismEnrichmentCDKN1B1.69
158Thrombotic microangiopathyEnrichmentATRIP1.69
159Oculomotor apraxiaEnrichmentATM1.69
160Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentCHEK11.69
161MicrocephalyEnrichmentABL1, NBN, SMC1A1.61
162Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1EnrichmentATRIP1.60
163Fanconi anemia, complementation group d2EnrichmentFANCD21.60
164Kearns-sayre syndromeEnrichmentRRM2B1.60
165Rhabdomyosarcoma 2EnrichmentTP531.60
166Breast-ovarian cancer, familial 2EnrichmentBRCA11.60
167LymphomaEnrichmentTP531.60
168GlioblastomaEnrichmentATM1.60
169Vascular dementiaEnrichmentATRIP1.60
170Acute megakaryocytic leukemiaEnrichmentTP531.60
171Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.60
172Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1EnrichmentRRM2B1.52
173Wilms tumor 5EnrichmentCHEK21.52
174Wiedemann-steiner syndromeEnrichmentSMC1A1.52
175Adrenocortical carcinomaEnrichmentTP531.52
176Clear cell renal cell carcinomaEnrichmentATM1.52
177Esophageal cancerEnrichmentTP531.45
178Leukemia, chronic myeloidEnrichmentABL11.45
179Renal cell carcinoma, papillary, 1EnrichmentATM1.45
180Essential thrombocythemiaEnrichmentTP531.45
181Gallbladder cancerEnrichmentTP531.45
182Moyamoya angiopathyEnrichmentABL11.45
183Primary ovarian insufficiencyEnrichmentCHEK2, NBN1.44
184Glioma susceptibility 1EnrichmentTP531.40
185Lymphoma, non-hodgkin, familialEnrichmentTP531.40
186Rett syndrome, congenital variantEnrichmentSMC1A1.40
187Cornelia de lange syndrome 1EnrichmentSMC1A1.35
188Primary hyperaldosteronismEnrichmentTP531.35
189Cornelia de lange syndromeEnrichmentSMC1A1.35
190Cowden syndromeEnrichmentAKT11.35
191Mitochondrial neurogastrointestinal encephalomyopathyEnrichmentRRM2B1.35
192Aplastic anemiaEnrichmentNBN1.30
193Aicardi-goutieres syndromeEnrichmentATRIP1.30
194MelanomaEnrichmentCHEK21.30
195Familial colorectal cancerEnrichmentTP531.30
196Immune deficiency diseaseEnrichmentATM1.26
197Xeroderma pigmentosum, variant typeEnrichmentDDB21.26
198Leukemia, acute lymphoblasticEnrichmentNBN1.26
199Myelodysplastic syndromeEnrichmentTP531.26
200MeningiomaEnrichmentAKT11.23
201Acute promyelocytic leukemiaEnrichmentPML1.19
202Premature menopauseEnrichmentNBN1.19
203Nk-cell enteropathyEnrichmentCHEK21.19
204Periventricular nodular heterotopiaEnrichmentBRCA11.16
205Heart diseaseEnrichmentABL11.16
206Renal cell carcinoma, nonpapillaryEnrichmentATM1.13
207Wilms tumor 1EnrichmentCHEK21.13
208Lynch syndromeEnrichmentCHEK21.13
209Melanoma, cutaneous malignant 1EnrichmentCDK41.08
210Polycystic liver diseaseEnrichmentCDC25A1.08
211Autosomal dominant polycystic liver diseaseEnrichmentCDC25A1.08
212Semilobar holoprosencephalyEnrichmentSMC1A1.06
213Behcet syndromeEnrichmentFAS1.03
214Parkinson's diseaseEnrichmentRFC11.03
215LissencephalyEnrichmentNBN0.99
216HepatoblastomaEnrichmentTP530.99
217Diamond-blackfan anemia 1EnrichmentTP530.96
218Parkinson disease, late-onsetEnrichmentRFC10.94
219Primary autosomal recessive microcephalyEnrichmentCDK60.82
220Diamond-blackfan anemiaEnrichmentTP530.77
221Systemic lupus erythematosusEnrichmentATRIP0.74
222Sensorineural hearing lossEnrichmentRRM2B0.66
223ThrombocytopeniaEnrichmentCYCS0.66
224Mitochondrial diseaseEnrichmentRRM2B0.44
225Congenital nervous system abnormalityEnrichmentSMC1A0.38
226Nervous system diseaseEnrichmentSMC1A0.38
227Retinitis pigmentosaEnrichmentRRM2B0.18
228Hereditary retinal dystrophyEnrichmentATRIP0.11
229Fundus dystrophyEnrichmentATRIP0.11

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