KEGG    Network variation - O-Glycan biosynthesis
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ENTRYnt06013
NameO-Glycan biosynthesis
CategoryPathway view; Glycan/glycoprotein metabolism
Pathwayhsa00515 Mannose type O-glycan biosynthesis
Modulehsa_M00872 O-glycan biosynthesis, mannose type (core M3)
DiseaseH02307 Muscular dystrophy-dystroglycanopathy
Display drug-target relation   disease type
N00627    Ser/Thr+Man-P-DolPOMT1/2POMGNT2B3GALNT2POMKG13092
    MDDGA1/B1/C1   POMT1*
    MDDGA2/B2/C2   POMT2*
    MDDGA3/B3/C3     POMGNT1*
    MDDGA8/C8     POMGNT2*
    MDDGA11       B3GALNT2*
    MDDGA12/C12         POMK*
N00698    CTP+Rib-ol-5PISPDCDP-Rib-ol
    MDDGC5   ISPD*
N00699    G13092+CDP-Rib-olFKTNFKRPTMEM5B4GAT1LARGE1/2G13099
    MDDGA4/B4/C4   FKTN*
    MDDGA5/B5/C5     FKRP*
    MDDGA10       TMEM5*
    MDDGA13         B4GAT1*
    MDDGA7/B6           LARGE1*

Disease nameDisease category
MDDGA1/B1/C1H02307Muscular dystrophy-dystroglycanopathyInherited metabolic disorder
MDDGA2/B2/C2H02307Muscular dystrophy-dystroglycanopathyInherited metabolic disorder
MDDGA3/B3/C3H02307Muscular dystrophy-dystroglycanopathyInherited metabolic disorder
MDDGA8/C8H00120Muscular dystrophy-dystroglycanopathy type AInherited metabolic disorder
H01959Muscular dystrophy-dystroglycanopathy type CInherited metabolic disorder
MDDGA11H00120Muscular dystrophy-dystroglycanopathy type AInherited metabolic disorder
MDDGA12/C12H00120Muscular dystrophy-dystroglycanopathy type AInherited metabolic disorder
H01959Muscular dystrophy-dystroglycanopathy type CInherited metabolic disorder
MDDGC5H01959Muscular dystrophy-dystroglycanopathy type CInherited metabolic disorder
MDDGA4/B4/C4H02307Muscular dystrophy-dystroglycanopathyInherited metabolic disorder
MDDGA5/B5/C5H02307Muscular dystrophy-dystroglycanopathyInherited metabolic disorder
MDDGA10H00120Muscular dystrophy-dystroglycanopathy type AInherited metabolic disorder
MDDGA13H00120Muscular dystrophy-dystroglycanopathy type AInherited metabolic disorder
MDDGA7/B6H00120Muscular dystrophy-dystroglycanopathy type AInherited metabolic disorder
H01960Muscular dystrophy-dystroglycanopathy type BInherited metabolic disorder