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ENTRY	nt06515
Name	Regulation of kinetochore-microtubule interactions
Category	Pathway view; Cellular processes
Pathway	hsa04110 Cell cycle
Disease	H01288 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

SSMGA	H02607	Short stature and microcephaly with genital anomalies
MCPH4	H00269	Primary microcephaly
MVA2	H01288	Mosaic variegated aneuploidy syndrome
PC	H00024	Prostate cancer
MCPH30	H00269	Primary microcephaly
CRC	H00020	Colorectal cancer
MVA1	H01288	Mosaic variegated aneuploidy syndrome
MVA3	H01288	Mosaic variegated aneuploidy syndrome
NSLH2	H02191	Noonan-like syndrome with loose anagen hair
MCPH13	H00269	Primary microcephaly
ROCHIS	H02585	Roifman-Chitayat syndrome
STROMS	H01814	Stromme syndrome
LIS4	H00268	Lissencephaly
MHAC	H01870	Microhydranencephaly
LIS1	H00268	Lissencephaly
HMN7B	H00856	Distal hereditary motor neuropathies
Perry	H00879	Perry syndrome
CMT2O	H00264	Charcot-Marie-Tooth disease
SMALED1	H00455	Spinal muscular atrophy
MRD13	H00773	Autosomal dominant intellectual developmental disorder
SRTD3	H02157	Short-rib thoracic dysplasia
NEDMIBA	H02461	Neurodevelopmental disorder with microcephaly
SRTD15	H02157	Short-rib thoracic dysplasia
LIS3	H00268	Lissencephaly
KTCN	H00789	Keratoconus
ALS22	H00058	Amyotrophic lateral sclerosis (ALS)
MACTHC2	H01740	Macrothrombocytopenia
CDCBM6	H01881	Complex cortical dysplasia with other brain malformations
CSCSC1	H01579	Congenital symmetric circumferential skin creases
MACTHC1	H01740	Macrothrombocytopenia
CDCBM5	H01881	Complex cortical dysplasia with other brain malformations
CDCBM7	H01881	Complex cortical dysplasia with other brain malformations
CDCBM1	H01881	Complex cortical dysplasia with other brain malformations
CFEOM3A	H00838	Congenital fibrosis of the extraocular muscles
HLD6	H00679	Hypomyelinating leukodystrophy
DYT4	H00831	Primary dystonia
LCAEOD	H00837	Leber congenital amaurosis
FPVEPD	H02594	Congenital facial palsy with ptosis and velopharyngeal dysfunction
OOMD2	H01897	Oocyte maturation defect
MCPH3	H00269	Primary microcephaly
CDCBM4	H01881	Complex cortical dysplasia with other brain malformations
PAMDDFS	H02606	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
MCCRP3	H01880	Autosomal recessive microcephaly and chorioretinopathy
MCCRP1	H01880	Autosomal recessive microcephaly and chorioretinopathy
MRD56	H00773	Autosomal dominant intellectual developmental disorder
OCSKD	H02595	Oculoskeletodental syndrome
CDCBM3	H01881	Complex cortical dysplasia with other brain malformations