KEGG    Network variation - TGFB signaling
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ENTRYnt06507
NameTGFB signaling
CategoryPathway view; Signal transduction
Pathwayhsa04350
DiseaseH00800 Loeys-Dietz syndrome
H00482 Brachydactyly
H00211 Hereditary hemochromatosis
H00533 Hereditary hemorrhagic telangiectasia
Display drug-target relation   disease type
N00063   
    CED
    LDS4
    LDS5
    LDS1A/2A/AAT5
    LDS1B/2BAAT3
    CRC
    LDS3
    LDS6
N00531    HBV
N00507    HTLV-1
N01460   
    GPHYSD2/MFS
    GPHYSD3/DASS
 
N01456   
    FOP
N01459   
    HTX5
    HTX4
 
N01453   
    BDA2
    BDA1C/BDA2/AMD2/SYNS2/SYM1B
    SYNS4
    JPS/HMPS
    BDA1D/BDA2/AMD3
N01428   
    BDB2/SYNS1/SYM1A/TCC
    STHAG9
 
N01458   
    HFE2B
N01461   
    HFE2A
    HFE1
    HFE3
 
N01426   
    HHT5
    PPH1
    HHT2
    PPH2
    JPHT/JPS/MYHRS
N01462   
    HHT1
 
N01455   
    ODG2
 
N01454   
    PMDS1
    PMDS2
 
N01457   
    MSLHP

CEDH00434Camurati-Engelmann disease
LDS4H00800Loeys-Dietz syndrome
LDS5H00800Loeys-Dietz syndrome
LDS1AH00800Loeys-Dietz syndrome
2AH00801Familial thoracic aortic aneurysm and dissection
LDS1BH00800Loeys-Dietz syndrome
2BAAT3H00801Familial thoracic aortic aneurysm and dissection
CRCH00020Colorectal cancer
LDS3H00800Loeys-Dietz syndrome
LDS6H00800Loeys-Dietz syndrome
HBVH00048Hepatocellular carcinoma
HTLV-1H00009Adult T-cell leukemia
GPHYSD2H00900Geleophysic dysplasia
MFSH00653Marfan syndrome
GPHYSD3H00900Geleophysic dysplasia
DASSH00625Tooth agenesis
FOPH00430Fibrodysplasia ossificans progressiva
HTX5H00632Heterotaxy
HTX4H00632Heterotaxy
BDA2H00482Brachydactyly
BDA1CH00482Brachydactyly
AMD2H00484Multiple synostosis syndrome
SYNS2H00851Proximal symphalangism
SYNS4H00484Multiple synostosis syndrome
JPSH01023Juvenile polyposis syndrome
HMPSH01024Hereditary mixed polyposis syndrome
BDA1DH00482Brachydactyly
BDB2H00482Brachydactyly
SYNS1H00484Multiple synostosis syndrome
SYM1AH00851Proximal symphalangism
TCCH00778Tarsal-carpal coalition syndrome
STHAG9H00625Tooth agenesis
HFE2BH00211Hemochromatosis
HFE2AH00211Hemochromatosis
HFE1H00211Hemochromatosis
HFE3H00211Hemochromatosis
HHT5H00533Hereditary hemorrhagic telangiectasia
PPH1H01619Primary pulmonary hypertension
HHT2H00533Hereditary hemorrhagic telangiectasia
PPH2H01619Primary pulmonary hypertension
JPHTH00533Hereditary hemorrhagic telangiectasia
MYHRSH02102Myhre syndrome
HHT1H00533Hereditary hemorrhagic telangiectasia
ODG2H00599Ovarian dysgenesis
PMDS1H00609Persistent Mullerian duct syndrome
PMDS2H00609Persistent Mullerian duct syndrome
MSLHPH02452Muscle hypertrophy