O-linked glycosylation

Pathway network for the O-linked glycosylation SuperPath

Sources:
  • Reactome
  • PubChem

Pathways in the O-linked glycosylation SuperPath

#NameSourceGenes
1O-linked glycosylationReactome
2O-linked glycosylation of mucinsReactome
3Defective C1GALT1C1 causes TNPSReactome
4Defective GALNT12 causes CRCS1Reactome
5Defective GALNT3 causes HFTCReactome
6DAG1 glycosylationsReactome
7Matriglycan biosynthesis on DAG1Reactome
8mucin core 1 and core 2 O-glycosylationPubChem
9α-dystroglycan glycosylationPubChem
10DAG1 core M3 glycosylationsReactome
11DAG1 core M2 glycosylationsReactome
12DAG1 core M1 glycosylationsReactome
13Defective POMGNT1 causes MDDGA3, MDDGB3 and MDDGC3Reactome
14Defective LARGE causes MDDGA6 and MDDGB6Reactome
15mucin core 3 and core 4 O-glycosylationPubChem

Gene overlap in member pathways for O-linked glycosylation SuperPath

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

Disorders associated with O-linked glycosylation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1HyperphosphatemiaDirect
2Muscular dystrophy-dystroglycanopathy , type b, 1Direct
3Congenital muscular dystrophyDirect
4Walker-warburg syndromeEnrichmentB3GALNT2, B4GAT1, CRPPA, DAG1, FKRP, FKTN, LARGE1, POMGNT1, POMGNT2, POMK, POMT1, POMT2, RXYLT116.00
5Muscle eye brain diseaseEnrichmentB3GALNT2, CRPPA, FKRP, FKTN, LARGE1, POMGNT1, POMT1, POMT216.00
6Congenital muscular dystrophy with cerebellar involvementEnrichmentFKRP, POMGNT1, POMK, POMT1, POMT216.00
7Muscular dystrophy-dystroglycanopathy , type a, 1EnrichmentB4GAT1, FKRP, FKTN, POMT1, POMT211.09
8Congenital muscular dystrophy without intellectual disabilityEnrichmentCRPPA, FKRP, FKTN, POMT111.00
9Congenital muscular dystrophy with intellectual disabilityEnrichmentFKRP, LARGE1, POMT1, POMT210.72
10Muscular dystrophy-dystroglycanopathyEnrichmentB3GALNT2, CRPPA, FKRP, POMGNT19.99
11Congenital muscular dystrophy due to dystroglycanopathyEnrichmentB3GALNT2, CRPPA, FKRP, POMGNT19.99
12Autosomal recessive limb-girdle muscular dystrophyEnrichmentFKRP, POMGNT1, POMT1, POMT28.08
13Muscular dystrophy-dystroglycanopathy , type c, 12EnrichmentPOMK, POMT16.79
14Congenital muscular dystrophy-dystroglycanopathy type aEnrichmentPOMGNT1, POMT26.71
15Muscular dystrophy-dystroglycanopathy , type a, 4EnrichmentFKRP, FKTN6.64
16Muscular dystrophy-dystroglycanopathy , type a, 8EnrichmentCRPPA, POMGNT25.30
17Ehlers-danlos syndrome, dermatosparaxis typeEnrichmentADAMTS2, ADAMTSL24.07
18Muscular dystrophy-dystroglycanopathy , type a, 9EnrichmentDAG13.53
19Muscular dystrophy-dystroglycanopathy , type c, 1EnrichmentPOMT13.53
20Muscular dystrophy-dystroglycanopathy , type c, 9EnrichmentDAG13.53
21Muscle-eye-brain disease with bilateral multicystic leucodystrophyEnrichmentDAG13.53
22Congenital nervous system abnormalityEnrichmentPOMGNT1, POMT13.44
23Nervous system diseaseEnrichmentPOMGNT1, POMT13.44
24Muscular dystrophy-dystroglycanopathy , type a, 12EnrichmentPOMK3.35
25Muscular dystrophy-dystroglycanopathy , type c, 8EnrichmentPOMGNT23.35
26Muscular dystrophyEnrichmentFKRP, POMT23.35
27Weill-marchesani syndromeEnrichmentADAMTS10, ADAMTS173.29
28Muscular dystrophy-dystroglycanopathy , type a, 6EnrichmentLARGE13.29
29Cardiomyopathy, dilated, 1xEnrichmentFKTN3.29
30Muscular dystrophy-dystroglycanopathy , type a, 13EnrichmentB4GAT13.29
31Muscular dystrophy-dystroglycanopathy , type b, 6EnrichmentLARGE13.29
32Muscular dystrophy-dystroglycanopathy , type b, 5EnrichmentFKRP3.29
33Muscular dystrophy-dystroglycanopathy , type a, 5EnrichmentFKRP3.29
34Muscular dystrophy-dystroglycanopathy , type a, 10EnrichmentRXYLT13.29
35Muscular dystrophy-dystroglycanopathy , type b, 4EnrichmentFKTN3.29
36Muscular dystrophy-dystroglycanopathy , type c, 4EnrichmentFKTN3.29
37Muscular dystrophy-dystroglycanopathy , type a, 3EnrichmentPOMGNT13.23
38Muscular dystrophy-dystroglycanopathy , type b, 3EnrichmentPOMGNT13.23
39Muscular dystrophy-dystroglycanopathy , type c, 2EnrichmentPOMT23.23
40Muscular dystrophy-dystroglycanopathy , type a, 2EnrichmentPOMT23.23
41Muscular dystrophy-dystroglycanopathy , type b, 2EnrichmentPOMT23.23
42Retinitis pigmentosa 76EnrichmentPOMGNT13.23
43Congenital muscular dystrophy-dystroglycanopathy type a3EnrichmentPOMGNT13.23
44Childhood-onset schizophreniaEnrichmentB3GNT6, GALNT43.21
45Muscular dystrophy-dystroglycanopathy , type c, 3EnrichmentPOMGNT13.05
46Muscular dystrophy-dystroglycanopathy , type a, 11EnrichmentB3GALNT23.05
47Congenital muscular dystrophy-dystroglycanopathy type a11EnrichmentB3GALNT23.05
48Congenital disorder of glycosylation, type iifEnrichmentSLC35A13.05
49Neuronopathy, distal hereditary motor, autosomal dominant 3EnrichmentFKRP2.99
50Tubulointerstitial kidney disease, autosomal dominant 2EnrichmentMUC12.88
51Colorectal cancer 1EnrichmentGALNT122.88
52Extrinsic allergic alveolitisEnrichmentMUC5B2.88
53Tn polyagglutination syndromeEnrichmentC1GALT1C12.85
54Hemolytic uremic syndrome, atypical, 8, with rhizomelic short statureEnrichmentC1GALT1C12.85
55Muscular dystrophy-dystroglycanopathy , type c, 5EnrichmentFKRP2.81
56Muscular dystrophy, congenital, due to integrin alpha-7 deficiencyEnrichmentCRPPA2.81
57Nizon-isidor syndromeEnrichmentFKRP2.81
58Muscular dystrophy-dystroglycanopathy , type c, 7EnrichmentCRPPA2.69
59Congenital muscular dystrophy-dystroglycanopathy type a7EnrichmentCRPPA2.69
60Muscular dystrophy-dystroglycanopathy , type a, 7EnrichmentCRPPA2.69
61Panbronchiolitis, diffuseEnrichmentMUC5B2.58
62HydrocephalusEnrichmentPOMGNT12.35
63Limb-girdle muscular dystrophyEnrichmentFKRP2.33
64Creatine phosphokinase, elevated serumEnrichmentDAG12.33
65Hydrocephalus, congenital, 1EnrichmentPOMT12.33
66Isolated elevated serum creatine phosphokinase levelsEnrichmentDAG12.33
67Intellectual developmental disorder, autosomal recessive 12EnrichmentST3GAL32.32
68Congenital disorder of glycosylation, type iitEnrichmentGALNT22.32
69St3gal3-cdgEnrichmentST3GAL32.32
70Pulmonary fibrosisEnrichmentMUC5B2.10
71Atypical hemolytic-uremic syndromeEnrichmentADAMTS13, C1GALT1C12.08
72Geleophysic dysplasia 1EnrichmentADAMTSL22.03
73Lethal short-limb skeletal dysplasia, al gazali typeEnrichmentADAMTSL22.03
74Microcornea, myopic chorioretinal atrophy, and telecanthusEnrichmentADAMTS182.03
75Hennekam lymphangiectasia-lymphedema syndrome 3EnrichmentADAMTS32.03
76Properdin deficiency, x-linkedEnrichmentCFP2.03
77Aortic aneurysm, familial thoracic 12EnrichmentTHSD42.03
78Arthrogryposis, distal, type 12EnrichmentADAMTS152.03
79Lymphatic malformation 13EnrichmentTHSD12.03
80Aneurysm, intracranial berry, 12EnrichmentTHSD12.03
81Cardiac valvular dysplasia 2EnrichmentADAMTS192.03
82Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndromeEnrichmentADAMTSL12.03
83Deafness, autosomal dominant 64EnrichmentB3GNT42.02
84Developmental and epileptic encephalopathy 15EnrichmentST3GAL32.02
85Tumoral calcinosis, hyperphosphatemic, familial, 1EnrichmentGALNT31.84
86Cone-rod dystrophy 20EnrichmentPOC1B-GALNT41.84
87Retinitis pigmentosaEnrichmentLARGE1, POMGNT11.84
88AsthmaEnrichmentMUC71.84
89Primary ovarian insufficiencyEnrichmentADAMTS1, ADAMTS6, THBS11.76
90Cri-du-chat syndromeEnrichmentSEMA5A1.73
91Ectopia lentis et pupillaeEnrichmentADAMTSL41.73
92Craniosynostosis with ectopia lentisEnrichmentADAMTSL41.73
93Thrombotic thrombocytopenic purpura, hereditaryEnrichmentADAMTS131.73
94Ectopia lentis 2, isolated, autosomal recessiveEnrichmentADAMTSL41.73
95Thrombotic thrombocytopenic purpuraEnrichmentADAMTS131.73
96MyopathyEnrichmentFKRP1.69
97Interstitial lung disease 2EnrichmentMUC5B1.65
98Autosomal recessive non-syndromic intellectual disabilityEnrichmentB3GALNT21.60
99Familial isolated dilated cardiomyopathyEnrichmentFKTN1.57
100Weill-marchesani syndrome 4EnrichmentADAMTS171.56
101Ehlers-danlos syndrome, classic-like, 3EnrichmentTHBS21.56
102Weill-marchesani syndrome 1EnrichmentADAMTS101.56
103Isolated ectopia lentisEnrichmentADAMTSL41.56
104Hennekam syndromeEnrichmentADAMTS31.56
105Geleophysic dysplasiaEnrichmentADAMTSL21.56
106Severe covid-19EnrichmentMUC5B1.42
107Dilated cardiomyopathyEnrichmentFKTN1.39
108Familial cerebral saccular aneurysmEnrichmentTHSD11.34
10946,xy disorder of sex developmentEnrichmentADAMTS161.26
110Intervertebral disc diseaseEnrichmentTHBS21.20
111Hereditary retinal dystrophyEnrichmentPOMGNT11.08
112Fundus dystrophyEnrichmentPOMGNT11.08
113Peters-plus syndromeEnrichmentB3GLCT1.05
114Ovarian cancerEnrichmentMUC160.90
115Anterior segment dysgenesisEnrichmentADAMTS170.88
116Male infertilityEnrichmentGALNTL50.82
117Developmental and epileptic encephalopathyEnrichmentST3GAL30.80
118Ehlers-danlos syndromeEnrichmentTHBS20.79
119Non-immune hydrops fetalisEnrichmentTHSD10.60
120NephronophthisisEnrichmentADAMTS90.58
121Familial thoracic aortic aneurysm and aortic dissectionEnrichmentTHSD40.47
122ThrombocytopeniaEnrichmentADAMTS130.44

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