Acyl chain remodelling of PE

Pathway network for the Acyl chain remodelling of PE SuperPath

Sources:
  • Reactome
  • WikiPathways

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

Disorders associated with Acyl chain remodelling of PE SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Bladder cancerEnrichmentCDKN1A, HRAS, TP535.01
2Lip and oral cavity carcinomaEnrichmentHRAS, TP533.87
3RhabdomyosarcomaEnrichmentHRAS, TP533.61
4Osteopetrosis and infantile neuroaxonal dystrophyEnrichmentPLA2G62.83
5Hypertrophic osteoarthropathy, primary, autosomal dominantEnrichmentSLCO2A12.83
6Fleck retina, familial benignEnrichmentPLA2G52.83
7Neurodegeneration with brain iron accumulation 2aEnrichmentPLA2G62.83
8Bone marrow failure syndrome 5EnrichmentTP532.83
9Papilloma of choroid plexusEnrichmentTP532.83
10Basal cell carcinoma 7EnrichmentTP532.83
11Anaplastic thyroid carcinomaEnrichmentTP532.83
12Parkinson disease 14, autosomal recessiveEnrichmentPLA2G62.83
13Neurodegeneration with brain iron accumulation 2bEnrichmentPLA2G62.83
14Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorderEnrichmentPLA2G4A2.83
15Ductal carcinoma in situEnrichmentTP532.83
16Platelet-activating factor acetylhydrolase deficiencyEnrichmentPLA2G72.83
17Gastrointestinal ulceration, recurrent, with dysfunctional plateletsEnrichmentPLA2G4A2.83
18Chronic enteropathy associated with slco2a1 geneEnrichmentSLCO2A12.83
19Thyroid gland undifferentiated carcinomaEnrichmentTP532.83
20Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.83
21Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.83
22Choroid plexus cancerEnrichmentTP532.83
23AtherosclerosisEnrichmentALOX52.83
24Pleomorphic xanthoastrocytomaEnrichmentTP532.83
25Cryptogenic multifocal ulcerous stenosing enteritisEnrichmentPLA2G4A2.83
26Phakomatosis pigmentokeratoticaEnrichmentHRAS2.83
27Familial benign flecked retinaEnrichmentPLA2G52.83
28Lipodystrophy, familial partial, type 9EnrichmentPLAAT32.79
29Mitochondrial myopathy with lactic acidosisEnrichmentPNPLA82.70
30Adrenocortical carcinoma, hereditaryEnrichmentTP532.53
31Costello syndromeEnrichmentHRAS2.53
32Cervical cancerEnrichmentTP532.53
33Lymphoma, hodgkin, classicEnrichmentTP532.53
34Phoar2-enteropathy syndromeEnrichmentSLCO2A12.53
35Congenital fibrosarcomaEnrichmentTP532.53
36Li-fraumeni syndrome 1EnrichmentTP532.53
37SarcomaEnrichmentTP532.53
38Primary hypertrophic osteoarthropathyEnrichmentSLCO2A12.53
39Cervix carcinomaEnrichmentTP532.53
40Hodgkin's lymphomaEnrichmentTP532.53
41Pleomorphic rhabdomyosarcomaEnrichmentTP532.53
42Infantile osteopetrosis with neuroaxonal dysplasiaEnrichmentPLA2G62.53
43Wooly hair nevusEnrichmentHRAS2.53
44Bardet-biedl syndrome 10EnrichmentOSBPL82.49
45Late-onset retinal degenerationEnrichmentPLA2G52.35
46Osteogenic sarcomaEnrichmentTP532.35
47Nasopharyngeal carcinomaEnrichmentTP532.35
48Hypertrophic osteoarthropathy, primary, autosomal recessive, 1EnrichmentSLCO2A12.35
49Large congenital melanocytic nevusEnrichmentHRAS2.35
50Atypical teratoid rhabdoid tumorEnrichmentTP532.35
51Anaplastic astrocytomaEnrichmentTP532.35
52Squamous cell carcinomaEnrichmentTP532.35
53AdenocarcinomaEnrichmentTP532.35
54Bone osteosarcomaEnrichmentTP532.35
55SpermatocytomaEnrichmentHRAS2.35
56Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS2.23
57Small cell cancer of the lungEnrichmentTP532.23
58Thyroid cancer, nonmedullary, 1EnrichmentTP532.23
59Lung sarcomatoid carcinomaEnrichmentTP532.23
60Embryonal rhabdomyosarcomaEnrichmentTP532.23
61Epidermolytic nevusEnrichmentHRAS2.23
62Multicentric osteolysis, nodulosis, and arthropathyEnrichmentLPCAT22.22
63Rhabdomyosarcoma 2EnrichmentTP532.13
64LymphomaEnrichmentTP532.13
65Acute megakaryocytic leukemiaEnrichmentTP532.13
66Li-fraumeni syndromeEnrichmentTP532.05
67Adrenocortical carcinomaEnrichmentTP532.05
68Breast adenocarcinomaEnrichmentTP532.05
69Esophageal cancerEnrichmentTP531.99
70Nevus, epidermalEnrichmentHRAS1.99
71Multiple endocrine neoplasia, type iEnrichmentCDKN1A1.99
72Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.99
73Squamous cell carcinoma, head and neckEnrichmentTP531.99
74Noonan syndrome 3EnrichmentHRAS1.99
75Essential thrombocythemiaEnrichmentTP531.99
76Gallbladder cancerEnrichmentTP531.99
77Follicular thyroid carcinomaEnrichmentHRAS1.99
78B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.99
79Melanocytic nevus syndrome, congenitalEnrichmentHRAS1.93
80Glioma susceptibility 1EnrichmentTP531.93
81Lymphoma, non-hodgkin, familialEnrichmentTP531.93
82Arteriovenous malformationEnrichmentHRAS1.88
83Adult hepatocellular carcinomaEnrichmentTP531.88
84Primary hyperaldosteronismEnrichmentTP531.88
85Leukemia, chronic lymphocyticEnrichmentTP531.83
86Myopathy, x-linked, with excessive autophagyEnrichmentHRAS1.83
87Neurodegeneration with brain iron accumulationEnrichmentPLA2G61.83
88Familial colorectal cancerEnrichmentTP531.83
89AsthmaEnrichmentALOX51.79
90Myelodysplastic syndromeEnrichmentTP531.79
91Lung non-small cell carcinomaEnrichmentHRAS1.79
92Lung cancer susceptibility 3EnrichmentTP531.69
93Noonan syndrome and noonan-related syndromeEnrichmentHRAS1.66
94Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delayEnrichmentPLA2G61.63
95GliosarcomaEnrichmentTP531.63
96Giant cell glioblastomaEnrichmentTP531.61
97Diffuse large b-cell lymphomaEnrichmentTP531.56
98HepatoblastomaEnrichmentTP531.52
99Hepatocellular carcinomaEnrichmentTP531.50
100Diamond-blackfan anemia 1EnrichmentTP531.48
101Noonan syndrome 1EnrichmentHRAS1.48
102Pancreatic cancerEnrichmentTP531.44
103Hydrops fetalis, nonimmuneEnrichmentHRAS1.42
104RasopathyEnrichmentHRAS1.42
105Prostate cancerEnrichmentTP531.38
106Differentiated thyroid carcinomaEnrichmentHRAS1.38
107Non-immune hydrops fetalisEnrichmentHRAS1.35
108Diamond-blackfan anemiaEnrichmentTP531.29
109Leukemia, acute myeloidEnrichmentTP531.24
110Gastric cancerEnrichmentTP531.21
111Hereditary breast carcinomaEnrichmentTP531.20
112Bardet-biedl syndromeEnrichmentOSBPL81.18
113Spastic ataxiaEnrichmentPLA2G61.12
114Hereditary breast ovarian cancer syndromeEnrichmentTP531.11
115Myeloma, multipleEnrichmentTP531.10
116Breast cancerEnrichmentTP530.98
117Colorectal cancerEnrichmentTP530.92
118Ovarian cancerEnrichmentTP530.86
119Congenital nervous system abnormalityEnrichmentPLA2G60.84
120Nervous system diseaseEnrichmentPLA2G60.84
121MicrocephalyEnrichmentPLA2G60.78
122Inherited cancer-predisposing syndromeEnrichmentTP530.75
123Hereditary retinal dystrophyEnrichmentOSBPL80.42
124Fundus dystrophyEnrichmentOSBPL80.42

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