KEGG    Network variation - Regulation of kinetochore-microtubule interactions
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ENTRYnt06515
NameRegulation of kinetochore-microtubule interactions
CategoryPathway view; Cellular processes
Pathwayhsa04110
DiseaseH01288 Mosaic variegated aneuploidy syndrome
H00268 Lissencephaly
H00269 Primary microcephaly
H01881 Complex cortical dysplasia with other brain malformations
Display drug-target relation   disease type
N01525   
    SSMGA
 
N01526   
    MCPH4
 
N01532   
    MVA2
    PC
 
N01529   
    MCPH30/CRC
    MVA1/CRC
 
N01533   
    MVA3
 
N01536   
    NSLH2
 
N01531   
    CRC
    MCPH13
    ROCHIS
 
N01534   
    STROMS
    LIS4/MHAC
    LIS1
    HMN7B/Perry
    CMT2O/SMALED1/MRD13
    SRTD3
    NEDMIBA
    SRTD15
 
N01535   
    LIS3
    KTCN
    ALS22
    MACTHC2
    CDCBM6/CSCSC1
    MACTHC1
    CDCBM5
    CDCBM7
    CDCBM1/CFEOM3A
    HLD6/DYT4
    LCAEOD
    FPVEPD
    OOMD2
 
N01544   
    MCPH3
N01549   
    CDCBM4
    PAMDDFS
    MCCRP3
    MCCRP1
 
N01547   
N01548   
    MRD56
    OCSKD
 
N01553   
 
N01561   
 
N01562   
N01563   
    CDCBM3

SSMGAH02607Short stature and microcephaly with genital anomalies
MCPH4H00269Primary microcephaly
MVA2H01288Mosaic variegated aneuploidy syndrome
PCH00024Prostate cancer
MCPH30H00269Primary microcephaly
CRCH00020Colorectal cancer
MVA1H01288Mosaic variegated aneuploidy syndrome
MVA3H01288Mosaic variegated aneuploidy syndrome
NSLH2H02191Noonan-like syndrome with loose anagen hair
MCPH13H00269Primary microcephaly
ROCHISH02585Roifman-Chitayat syndrome
STROMSH01814Stromme syndrome
LIS4H00268Lissencephaly
MHACH01870Microhydranencephaly
LIS1H00268Lissencephaly
HMN7BH00856Distal hereditary motor neuropathies
PerryH00879Perry syndrome
CMT2OH00264Charcot-Marie-Tooth disease
SMALED1H00455Spinal muscular atrophy
MRD13H00773Autosomal dominant intellectual developmental disorder
SRTD3H02157Short-rib thoracic dysplasia
NEDMIBAH02461Neurodevelopmental disorder with microcephaly
SRTD15H02157Short-rib thoracic dysplasia
LIS3H00268Lissencephaly
KTCNH00789Keratoconus
ALS22H00058Amyotrophic lateral sclerosis (ALS)
MACTHC2H01740Macrothrombocytopenia
CDCBM6H01881Complex cortical dysplasia with other brain malformations
CSCSC1H01579Congenital symmetric circumferential skin creases
MACTHC1H01740Macrothrombocytopenia
CDCBM5H01881Complex cortical dysplasia with other brain malformations
CDCBM7H01881Complex cortical dysplasia with other brain malformations
CDCBM1H01881Complex cortical dysplasia with other brain malformations
CFEOM3AH00838Congenital fibrosis of the extraocular muscles
HLD6H00679Hypomyelinating leukodystrophy
DYT4H00831Primary dystonia
LCAEODH00837Leber congenital amaurosis
FPVEPDH02594Congenital facial palsy with ptosis and velopharyngeal dysfunction
OOMD2H01897Oocyte maturation defect
MCPH3H00269Primary microcephaly
CDCBM4H01881Complex cortical dysplasia with other brain malformations
PAMDDFSH02606Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
MCCRP3H01880Autosomal recessive microcephaly and chorioretinopathy
MCCRP1H01880Autosomal recessive microcephaly and chorioretinopathy
MRD56H00773Autosomal dominant intellectual developmental disorder
OCSKDH02595Oculoskeletodental syndrome
CDCBM3H01881Complex cortical dysplasia with other brain malformations