Ubiquitination Cascade

No Pathway Network information available for Ubiquitination Cascade

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

Disorders associated with Ubiquitination Cascade SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Intellectual developmental disorder, x-linked 99EnrichmentUSP9X2.66
2Fanconi anemia, complementation group tEnrichmentUBE2T2.66
3Immunodeficiency 107 invasive staphylococcus aureus infectionEnrichmentOTULIN2.66
4Intellectual developmental disorder, x-linked, syndromic, nascimento typeEnrichmentUBE2A2.66
5Intellectual developmental disorder, x-linked 99, syndromic, female-restrictedEnrichmentUSP9X2.66
6Syndromic x-linked intellectual disability nascimento typeEnrichmentUBE2A2.66
7Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessiveEnrichmentOTULIN2.66
8Female-restricted syndromic x-linked intellectual disability 99EnrichmentUSP9X2.66
9Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominantEnrichmentOTULIN2.66
10Lymphoproliferative syndrome, x-linked, 2EnrichmentXIAP2.44
11Accelerated tumor formationEnrichmentMDM22.44
12Lessel-kubisch syndromeEnrichmentMDM22.44
13Cardiomyopathy, familial hypertrophic, 31EnrichmentTRIM632.44
14Autoimmune disease, multisystem, with facial dysmorphismEnrichmentITCH2.44
15Immunodeficiency 115 with autoinflammationEnrichmentRNF312.44
16Syndromic multisystem autoimmune disease due to itch deficiencyEnrichmentITCH2.44
1715q11q13 microduplication syndromeEnrichmentUBE3A2.44
18Vexas syndromeEnrichmentUBA12.35
19Spinal muscular atrophy, x-linked 2EnrichmentUBA12.35
20Hao-fountain syndromeEnrichmentUSP72.35
21Submucosal cleft palateEnrichmentUBB2.35
22Cleft hard palateEnrichmentUBB2.35
23Craniometaphyseal dysplasia, autosomal dominantEnrichmentOTULIN2.18
24Uvula, bifidEnrichmentUBB2.18
25Cleft soft palateEnrichmentUBB2.18
26Hyperpigmentation of the skinEnrichmentUSP9X2.18
27Cylindromatosis, familialEnrichmentCYLD2.14
28Trichoepithelioma, multiple familial, 1EnrichmentCYLD2.14
29Spinocerebellar ataxia 48EnrichmentSTUB12.14
30Frontotemporal dementia and/or amyotrophic lateral sclerosis 8EnrichmentCYLD2.14
31Brooke-spiegler syndromeEnrichmentCYLD2.14
32Microcephaly-capillary malformation syndromeEnrichmentSTAMBP2.14
33Angelman syndrome due to maternal 15q11q13 deletionEnrichmentUBE3A2.14
34Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosisEnrichmentRNF312.14
35Chondrocalcinosis 2EnrichmentOTULIN2.05
36Dedifferentiated liposarcomaEnrichmentMDM21.97
37Well-differentiated liposarcomaEnrichmentMDM21.97
38Angelman syndrome due to imprinting defect in 15q11-q13EnrichmentUBE3A1.97
39Lymphoproliferative syndrome 2EnrichmentXIAP1.84
40Angelman syndromeEnrichmentUBE3A1.67
41Li-fraumeni syndromeEnrichmentMDM21.67
42Spinocerebellar ataxia, autosomal recessive 16EnrichmentSTUB11.67
43Fanconi anemia, complementation group aEnrichmentUBE2T1.13
44Non-syndromic x-linked intellectual disabilityEnrichmentUSP9X1.12
45Systemic lupus erythematosusEnrichmentUBE2L31.08
46Autoinflammatory diseaseEnrichmentXIAP1.08
47Hypertrophic cardiomyopathyEnrichmentTRIM630.84
48Myeloma, multipleEnrichmentCYLD0.74
49Inherited cancer-predisposing syndromeEnrichmentCYLD0.42

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