Genotoxicity pathway

No Pathway Network information available for Genotoxicity pathway

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

Disorders associated with Genotoxicity pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Accelerated tumor formationEnrichmentMDM22.35
2Lessel-kubisch syndromeEnrichmentMDM22.35
3Mitochondrial dna depletion syndrome 8bEnrichmentRRM2B2.35
4Rahman syndromeEnrichmentH1-42.35
5Retinitis pigmentosa 31EnrichmentTOPORS2.35
6Microcephaly 13, primary, autosomal recessiveEnrichmentCENPE2.35
7Jansen-de vries syndromeEnrichmentPPM1D2.35
8Epilepsy, familial adult myoclonic, 7EnrichmentRAPGEF22.35
9Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic faciesEnrichmentSEL1L2.35
10Tayoun-maawali syndromeEnrichmentFBXO222.35
11Trim22-related inflammatory bowel diseaseEnrichmentTRIM222.35
12Rrm2b mitochondrial dna maintenance defectsEnrichmentRRM2B2.35
13Spinocerebellar ataxia 29EnrichmentITPR12.05
14Fanconi renotubular syndrome 1EnrichmentRRM2B2.05
15Osteopathia striata with cranial sclerosisEnrichmentAMER12.05
16Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunctionEnrichmentRRM2B2.05
17Xeroderma pigmentosum, complementation group eEnrichmentDDB22.05
18Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 5EnrichmentRRM2B2.05
19Aortic aneurysm, familial thoracic 2EnrichmentACTA22.05
20Mitochondrial dna depletion syndrome 8aEnrichmentRRM2B2.05
21Smooth muscle dysfunction syndromeEnrichmentACTA22.05
22Aortic aneurysm, familial thoracic 6EnrichmentACTA22.05
23Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 2EnrichmentRRM2B2.05
24Moyamoya disease 5EnrichmentACTA22.05
25Autoimmune disease, multisystem, infantile-onset, 3EnrichmentCBLB2.05
26Diamond-blackfan anemia 17EnrichmentRPS272.05
27Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemiaEnrichmentSEL1L2.05
28Xeroderma pigmentosum group eEnrichmentDDB22.05
29Gillespie syndromeEnrichmentITPR11.88
30Dedifferentiated liposarcomaEnrichmentMDM21.88
31Idiopathic camptocormiaEnrichmentRRM2B1.88
32Well-differentiated liposarcomaEnrichmentMDM21.88
33Autoimmune lymphoproliferative syndromeEnrichmentACTA21.76
34Spinocerebellar ataxia 15EnrichmentITPR11.76
35Kearns-sayre syndromeEnrichmentRRM2B1.66
36Li-fraumeni syndromeEnrichmentMDM21.58
37Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1EnrichmentRRM2B1.58
38Moyamoya disease 1EnrichmentACTA21.58
39Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR11.58
40Multiple endocrine neoplasia, type iEnrichmentCDKN1A1.51
41Mitochondrial neurogastrointestinal encephalomyopathyEnrichmentRRM2B1.41
42Orofaciodigital syndrome viEnrichmentTOPORS1.32
43Xeroderma pigmentosum, variant typeEnrichmentDDB21.32
44Multiple sclerosisEnrichmentITPR11.22
45Lung cancer susceptibility 3EnrichmentACTA21.22
46Seckel syndromeEnrichmentCENPE1.22
47Anterior segment dysgenesisEnrichmentITPR11.19
48Cleft palate, isolatedEnrichmentAMER11.14
49Auditory neuropathyEnrichmentH1-40.96
50Bladder cancerEnrichmentCDKN1A0.92
51Lung cancerEnrichmentACTA20.88
52Primary autosomal recessive microcephalyEnrichmentCENPE0.88
53Connective tissue diseaseEnrichmentACTA20.88
54Diamond-blackfan anemiaEnrichmentRPS270.83
55Familial thoracic aortic aneurysm and aortic dissectionEnrichmentACTA20.75
56Hereditary breast carcinomaEnrichmentPPM1D0.75
57Sensorineural hearing lossEnrichmentRRM2B0.72
58Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPM1D0.70
59Spastic ataxiaEnrichmentITPR10.68
60Myeloma, multipleEnrichmentH1-40.66
61Retinitis pigmentosaEnrichmentRRM2B, TOPORS0.62
62Breast cancerEnrichmentPPM1D0.55
63Colorectal cancerEnrichmentAMER10.49
64Mitochondrial diseaseEnrichmentRRM2B0.49
65Ovarian cancerEnrichmentPPM1D0.44
66Hereditary retinal dystrophyEnrichmentTOPORS0.14
67Fundus dystrophyEnrichmentTOPORS0.14

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