Fluoropyrimidine activity

Pathway network for the Fluoropyrimidine activity SuperPath

Sources:
  • WikiPathways
  • PharmGKB
  • PubChem

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

Disorders associated with Fluoropyrimidine activity SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1HepatoblastomaEnrichmentERCC2, TP533.99
2Bladder cancerEnrichmentERCC2, TP533.71
3Dihydropyrimidinase deficiencyEnrichmentDPYS3.43
4Beta-ureidopropionase deficiencyEnrichmentUPB13.43
51p21.3 microdeletion syndromeEnrichmentDPYD3.43
6Homocystinuria due to deficiency of n -methylenetetrahydrofolate reductase activityEnrichmentMTHFR3.13
7Bone marrow failure syndrome 5EnrichmentTP533.13
8Papilloma of choroid plexusEnrichmentTP533.13
9Basal cell carcinoma 7EnrichmentTP533.13
10Xeroderma pigmentosum, complementation group dEnrichmentERCC23.13
11Anaplastic thyroid carcinomaEnrichmentTP533.13
12Cerebrooculofacioskeletal syndrome 2EnrichmentERCC23.13
13Megaloblastic anemia due to dihydrofolate reductase deficiencyEnrichmentDHFR3.13
14Ductal carcinoma in situEnrichmentTP533.13
15Thyroid gland undifferentiated carcinomaEnrichmentTP533.13
16Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP533.13
17Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP533.13
18Choroid plexus cancerEnrichmentTP533.13
19Xeroderma pigmentosum group dEnrichmentERCC23.13
20Pleomorphic xanthoastrocytomaEnrichmentTP533.13
21Dihydropyrimidine dehydrogenase deficiencyEnrichmentDPYD2.96
22Breast cancerEnrichmentTP53, XRCC32.88
23Adrenocortical carcinoma, hereditaryEnrichmentTP532.83
24Cervical cancerEnrichmentTP532.83
25Melanoma, cutaneous malignant 6EnrichmentXRCC32.83
26Lymphoma, hodgkin, classicEnrichmentTP532.83
27Congenital fibrosarcomaEnrichmentTP532.83
28Li-fraumeni syndrome 1EnrichmentTP532.83
29SarcomaEnrichmentTP532.83
30Cervix carcinomaEnrichmentTP532.83
31Hodgkin's lymphomaEnrichmentTP532.83
32Dyskeratosis congenita, digenicEnrichmentTYMS2.83
33Isolated anencephalyEnrichmentMTHFR2.83
34Isolated exencephalyEnrichmentMTHFR2.83
35Pleomorphic rhabdomyosarcomaEnrichmentTP532.83
36Orotic aciduriaEnrichmentUMPS2.75
37Uric acid concentration, serum, quantitative trait locus 1EnrichmentABCG22.75
38Drug metabolism, altered, ces1-relatedEnrichmentCES12.75
39Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6EnrichmentRRM12.75
40Hemolytic disease of the fetusEnrichmentSLC29A12.75
41Blood group, junior systemEnrichmentABCG22.75
42Letrozole toxicityEnrichmentCYP2A62.75
43Trichothiodystrophy 1, photosensitiveEnrichmentERCC22.66
44Osteogenic sarcomaEnrichmentTP532.66
45Nasopharyngeal carcinomaEnrichmentTP532.66
46Familial adenomatous polyposis 4EnrichmentDHFR2.66
47Atypical teratoid rhabdoid tumorEnrichmentTP532.66
48Anaplastic astrocytomaEnrichmentTP532.66
49Squamous cell carcinomaEnrichmentTP532.66
50AdenocarcinomaEnrichmentTP532.66
51Bone osteosarcomaEnrichmentTP532.66
52Ovarian cancerEnrichmentERCC2, TP532.62
53Small cell cancer of the lungEnrichmentTP532.53
54Thyroid cancer, nonmedullary, 1EnrichmentTP532.53
55Neural tube defects, folate-sensitiveEnrichmentMTHFR2.53
56Lung sarcomatoid carcinomaEnrichmentTP532.53
57Embryonal rhabdomyosarcomaEnrichmentTP532.53
58CraniopharyngiomaEnrichmentERCC22.53
59Rhabdomyosarcoma 2EnrichmentTP532.43
60LymphomaEnrichmentTP532.43
61Acute megakaryocytic leukemiaEnrichmentTP532.43
62Xeroderma pigmentosum-cockayne syndrome complexEnrichmentERCC22.43
63Inherited cancer-predisposing syndromeEnrichmentDHFR, TP532.40
64Li-fraumeni syndromeEnrichmentTP532.35
65Cerebrooculofacioskeletal syndrome 1EnrichmentERCC22.35
66Adrenocortical carcinomaEnrichmentTP532.35
67Breast adenocarcinomaEnrichmentTP532.35
68Esophageal cancerEnrichmentTP532.29
69Thrombophilia due to thrombin defectEnrichmentMTHFR2.29
70Squamous cell carcinoma, head and neckEnrichmentTP532.29
71Essential thrombocythemiaEnrichmentTP532.29
72Gallbladder cancerEnrichmentTP532.29
73B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP532.29
74Coumarin resistanceEnrichmentCYP2A62.28
75Glioma susceptibility 1EnrichmentTP532.23
76Lymphoma, non-hodgkin, familialEnrichmentTP532.23
77Inflammatory bowel disease 1EnrichmentERCC22.18
78Adult hepatocellular carcinomaEnrichmentTP532.18
79Primary hyperaldosteronismEnrichmentTP532.18
80Hypotrichosis simplexEnrichmentERCC22.18
81TrichothiodystrophyEnrichmentERCC22.18
82Tobacco addictionEnrichmentCYP2A62.15
83Leukemia, chronic lymphocyticEnrichmentTP532.13
84Familial colorectal cancerEnrichmentTP532.13
85Xeroderma pigmentosum, variant typeEnrichmentERCC22.09
86Myelodysplastic syndromeEnrichmentTP532.09
87Lip and oral cavity carcinomaEnrichmentTP532.05
88Neural tube defectsEnrichmentMTHFR2.02
89Lung cancer susceptibility 3EnrichmentTP531.99
90Mitochondrial dna depletion syndrome 1EnrichmentTYMP1.98
91Corpus callosum, agenesis ofEnrichmentERCC21.96
92Isolated corpus callosum agenesisEnrichmentERCC21.96
93Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentERCC21.96
94RhabdomyosarcomaEnrichmentTP531.93
95GliosarcomaEnrichmentTP531.93
96Giant cell glioblastomaEnrichmentTP531.90
97Diffuse large b-cell lymphomaEnrichmentTP531.86
98Dyskeratosis congenitaEnrichmentTYMS1.86
99Mitochondrial dna depletion syndrome 4bEnrichmentTYMP1.85
100LeukodystrophyEnrichmentERCC21.83
101Endometrial cancerEnrichmentDHFR1.81
102Mitochondrial neurogastrointestinal encephalomyopathyEnrichmentTYMP1.80
103Hepatocellular carcinomaEnrichmentTP531.79
104Diamond-blackfan anemia 1EnrichmentTP531.77
105Pancreatic cancerEnrichmentTP531.74
106Prostate cancerEnrichmentTP531.67
107Diamond-blackfan anemiaEnrichmentTP531.58
108Leukemia, acute myeloidEnrichmentTP531.54
109Gastric cancerEnrichmentTP531.50
110West syndromeEnrichmentMTHFR1.50
111Hereditary breast carcinomaEnrichmentTP531.50
112Hereditary breast ovarian cancer syndromeEnrichmentTP531.40
113Myeloma, multipleEnrichmentTP531.39
114SchizophreniaEnrichmentMTHFR1.37
115Lung cancerEnrichmentCYP2A61.26
116Colorectal cancerEnrichmentTP531.21

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