Protein ubiquitination

No Pathway Network information available for Protein ubiquitination

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

Disorders associated with Protein ubiquitination SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Neonatal adrenoleukodystrophyEnrichmentPEX10, PEX12, PEX13, PEX14, PEX2, PEX516.00
2Peroxisome biogenesis disorder 1bEnrichmentPEX10, PEX12, PEX13, PEX14, PEX2, PEX510.56
3Zellweger syndromeEnrichmentPEX10, PEX12, PEX13, PEX14, PEX2, PEX510.56
4Zellweger spectrum disorderEnrichmentPEX10, PEX2, PEX55.39
5Peroxisome biogenesis disorder 2aEnrichmentPEX52.37
6Peroxisome biogenesis disorder 3bEnrichmentPEX122.37
7Parathyroid carcinomaEnrichmentCDC732.37
8Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1EnrichmentVCP2.37
9Hyperparathyroidism 2 with jaw tumorsEnrichmentCDC732.37
10Peroxisome biogenesis disorder 3aEnrichmentPEX122.37
11Intellectual developmental disorder, x-linked, syndromic, nascimento typeEnrichmentUBE2A2.37
12Syndromic x-linked intellectual disability nascimento typeEnrichmentUBE2A2.37
13Birdshot chorioretinopathyEnrichmentHLA-A2.37
14Peroxisome biogenesis disorder 6aEnrichmentPEX102.37
15Immunodeficiency 26 with or without neurologic abnormalitiesEnrichmentPRKDC2.37
16Peroxisome biogenesis disorder 6bEnrichmentPEX102.37
17Ataxia-telangiectasia-like disorder 2EnrichmentPCNA2.37
18Cdc73-related disordersEnrichmentCDC732.37
19Frontotemporal dementia and/or amyotrophic lateral sclerosis 6EnrichmentVCP2.37
20Multisystem proteinopathyEnrichmentVCP2.37
21Rhizomelic chondrodysplasia punctata, type 5EnrichmentPEX52.37
22Adult-onset distal myopathy due to vcp mutationEnrichmentVCP2.37
23Autosomal recessive ataxia due to pex10 deficiencyEnrichmentPEX102.37
24Autosomal recessive ataxia due to pex2 deficiencyEnrichmentPEX22.37
25Intellectual developmental disorder, x-linked 99EnrichmentUSP9X2.24
26Fanconi anemia, complementation group tEnrichmentUBE2T2.24
27Immunodeficiency 107 invasive staphylococcus aureus infectionEnrichmentOTULIN2.24
28Intellectual developmental disorder, x-linked 99, syndromic, female-restrictedEnrichmentUSP9X2.24
29Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessiveEnrichmentOTULIN2.24
30Female-restricted syndromic x-linked intellectual disability 99EnrichmentUSP9X2.24
31Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominantEnrichmentOTULIN2.24
32Severe cutaneous adverse reactionEnrichmentHLA-A2.07
33Amyotrophic lateral sclerosis 6 with or without frontotemporal dementiaEnrichmentVCP2.07
34Hyperparathyroidism 1EnrichmentCDC732.07
35Peroxisome biogenesis disorder 11aEnrichmentPEX132.07
36Peroxisome biogenesis disorder 13aEnrichmentPEX142.07
37Peroxisome biogenesis disorder 2bEnrichmentPEX52.07
38Peroxisome biogenesis disorder 11bEnrichmentPEX132.07
39Desanto-shinawi syndromeEnrichmentWAC2.07
40Submucosal cleft palateEnrichmentUBB2.07
41Desanto-shinawi syndrome due to wac point mutationEnrichmentWAC2.07
42Cleft hard palateEnrichmentUBB2.07
43Spastic paraplegia-paget disease of bone syndromeEnrichmentVCP2.07
44Vexas syndromeEnrichmentUBA11.94
45Spinal muscular atrophy, x-linked 2EnrichmentUBA11.94
46Hao-fountain syndromeEnrichmentUSP71.94
47Uvula, bifidEnrichmentUBB1.89
48Cleft soft palateEnrichmentUBB1.89
49Peroxisome biogenesis disorder 5bEnrichmentPEX21.89
50Peroxisome biogenesis disorder 5aEnrichmentPEX21.89
51Tessadori-bicknell-van haaften neurodevelopmental syndrome 4EnrichmentH2BC121.89
52Inclusion body myopathy with paget disease of bone and frontotemporal dementiaEnrichmentVCP1.89
53Parathyroid adenomaEnrichmentCDC731.89
54Familial isolated hyperparathyroidismEnrichmentCDC731.89
55Rhizomelic chondrodysplasia punctataEnrichmentPEX51.77
56Craniometaphyseal dysplasia, autosomal dominantEnrichmentOTULIN1.77
57Hyperpigmentation of the skinEnrichmentUSP9X1.77
58Dementia, lewy bodyEnrichmentVCP1.67
59Charcot-marie-tooth disease, axonal, type 2eEnrichmentVCP1.67
60Chondrocalcinosis 2EnrichmentOTULIN1.64
61Peroxisome biogenesis disorder 1aEnrichmentPEX51.60
62Multiple endocrine neoplasia, type iEnrichmentCDC731.53
63Progressive non-fluent aphasiaEnrichmentVCP1.42
64Behavioral variant of frontotemporal dementiaEnrichmentVCP1.42
65Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentVCP1.38
66Alzheimer's diseaseEnrichmentVCP1.27
67Wilms tumor 1EnrichmentCTR91.21
68Alzheimer disease, familial, 1EnrichmentVCP1.15
69Neuropathy, hereditary motor and sensory, okinawa typeEnrichmentVCP1.11
70Severe covid-19EnrichmentHLA-A0.93
71Systemic lupus erythematosusEnrichmentUBE2L30.81
72Hereditary breast carcinomaEnrichmentCDC730.76
73Fanconi anemia, complementation group aEnrichmentUBE2T0.74
74Non-syndromic x-linked intellectual disabilityEnrichmentUSP9X0.73
75Spastic ataxiaEnrichmentPEX100.69
76Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentLEO10.67
77Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentVCP0.66
78Breast cancerEnrichmentCDC730.56
79Complex neurodevelopmental disorderEnrichmentCTR90.38
80Inherited cancer-predisposing syndromeEnrichmentCDC730.36

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