TGFBR2 Kinase Domain Mutants in Cancer

Pathway network for the TGFBR2 Kinase Domain Mutants in Cancer SuperPath

Sources:
  • Reactome
  • WikiPathways

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

Disorders associated with TGFBR2 Kinase Domain Mutants in Cancer SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1InfluenzaDirect
2Loeys-dietz syndromeEnrichmentSMAD2, SMAD3, TGFBR1, TGFBR210.62
3Loeys-dietz syndrome 1EnrichmentSMAD2, TGFBR1, TGFBR210.25
4Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD2, SMAD3, TGFBR1, TGFBR28.84
5Loeys-dietz syndrome 2EnrichmentTGFBR1, TGFBR27.49
6Aortic aneurysmEnrichmentSMAD3, TGFBR16.01
7Marfan syndromeEnrichmentTGFBR1, TGFBR25.83
8Pseudomyogenic hemangioendotheliomaEnrichmentSERPINE1, WWTR15.53
9Ehlers-danlos syndromeEnrichmentSMAD3, TGFBR24.56
10Connective tissue diseaseEnrichmentSMAD3, TGFBR24.09
11Colorectal cancer, hereditary nonpolyposis, type 6EnrichmentTGFBR23.83
12Multiple self-healing squamous epitheliomaEnrichmentTGFBR13.66
13Camurati-engelmann disease 1EnrichmentTGFB13.53
14Microvascular complications of diabetes 5EnrichmentTGFBR23.53
15Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB13.53
16Camurati-engelmann diseaseEnrichmentTGFB13.53
17Loeys-dietz syndrome 6EnrichmentSMAD23.35
18Congenital heart defects, multiple types, 8, with or without heterotaxyEnrichmentSMAD23.35
19Inflammatory bowel disease 10EnrichmentATG16L13.29
20Plasminogen activator inhibitor-1 deficiencyEnrichmentSERPINE13.13
21Developmental and epileptic encephalopathy 56EnrichmentYWHAG3.13
22Congenital plasminogen activator inhibitor type 1 deficiencyEnrichmentSERPINE13.13
23Loeys-dietz syndrome 3EnrichmentSMAD33.05
24Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB13.05
25Il10-related early-onset inflammatory bowel diseaseEnrichmentTGFB13.05
26Esophageal cancerEnrichmentTGFBR22.99
27Classic ehlers-danlos syndromeEnrichmentTGFBR12.88
28Kyphomelic dysplasiaEnrichmentCCN22.83
29Spondyloepimetaphyseal dysplasia, li-shao-li typeEnrichmentCCN22.83
30Osteogenesis imperfecta, type xviiEnrichmentSPARC2.83
31Lynch syndromeEnrichmentTGFBR22.66
32Pectus excavatumEnrichmentTGFBR12.61
33Malignant epithelioid hemangioendotheliomaEnrichmentWWTR12.53
34Diffuse cutaneous systemic sclerosisEnrichmentCCN22.43
35Familial cerebral saccular aneurysmEnrichmentTGFBR32.43
36Familial thoracic aortic aneurysm and dissectionEnrichmentSMAD32.40
37Limited sclerodermaEnrichmentCCN22.35
38Cystic fibrosisEnrichmentTGFB12.33
39Aortic aneurysm, familial thoracic 1EnrichmentSMAD32.21
40Specific learning disabilityEnrichmentYWHAG2.09
41Osteogenesis imperfecta, type ivEnrichmentSPARC2.02
42Undetermined early-onset epileptic encephalopathyEnrichmentYWHAG1.39
43MicrocephalyEnrichmentYWHAG1.06

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