KEGG    Network variation - HH signaling
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ENTRYnt06501
NameHH signaling
CategoryPathway view; Signal transduction
Pathwayhsa04340 Hedgehog signaling pathway
DiseaseH00039 Basal cell carcinoma
H01835 Neuronal migration disorder
Display drug-target relation   disease type
N00062    HHPTCHSMO(SMO+EVC)(SUFU+KIF7)GLI(GLI1,PTCH,HHIP)
    HPE3/MCOPCB5 SHH*
    BDA1/ACFD IHH*
    BCC1   PTCH1*
      PTCH1*
    BCC1   PTCH2*
    BCC1     SMO*
    EVC/WAD       EVC*
    EVC/WAD       EVC2*
            SUFU*
    JBTS12/ACLS/HLS2         KIF7*
    PAPA8/PPD1           GLI1*
    HPE9           GLI2*
    GCPS/PAPA1/PAPB/PPD4/PHS           GLI3*
 
N01537    HHATHHDISP1SCUBE2HH(extracellular)
    NNMS HHAT*
 
N01538    ((CDON,BOC),GAS1,L..(HH+PTCH)
    HPE11 CDON*
    DBS LRP2*

Disease nameDisease category
HPE3/MCOPCB5H00267HoloprosencephalyCongenital malformation
H01027MicrophthalmiaCongenital malformation
BDA1/ACFDH00482BrachydactylyCongenital malformation
H00675Acrocapitofemoral dysplasiaCongenital malformation
BCC1H00039Basal cell carcinomaCancer
HPE7/BCNSH00267HoloprosencephalyCongenital malformation
H00895Basal cell nevus syndromeCongenital malformation
EVC/WADH00503Ellis-van Creveld syndromeCongenital malformation
H02158Weyers acrofacial dysostosisCongenital malformation
BCNS/JBTS32H00895Basal cell nevus syndromeCongenital malformation
H00530Joubert syndrome and related disordersCongenital malformation
JBTS12/ACLS/HLS2H00530Joubert syndrome and related disordersCongenital malformation
H00263Acrocallosal syndromeCongenital malformation
H01265Hydrolethalus syndromeCongenital malformation
PAPA8/PPD1H01852Postaxial polydactylyCongenital malformation
H02332Preaxial polydactylyCongenital malformation
HPE9H00267HoloprosencephalyCongenital malformation
GCPS/PAPA1/PAPB/PPD4/PHSH02161Greig cephalopolysyndactyly syndromeCongenital malformation
H01852Postaxial polydactylyCongenital malformation
H02332Preaxial polydactylyCongenital malformation
H00502Pallister-Hall syndromeCongenital malformation
NNMSH02479Nivelon-Nivelon-Mabille syndromeCongenital malformation
HPE11H00267HoloprosencephalyCongenital malformation
DBSH00886Donnai-Barrow syndromeCongenital malformation