Publication for CIT and ASPM

Species	Symbol	Function*	Entrez Gene ID*	Other ID	Gene coexpression	CoexViewer
hsa	CIT	citron rho-interacting serine/threonine kinase	11113			[link]
hsa	ASPM	assembly factor for spindle microtubules	259266

Pubmed ID	Priority	Text
26743006	0.97	ASPM, CENPF, CIT, HMMR, PBK, PRC1, SKA3 and UBE2C) and four of our previously identified CREB1/FoxA1 target genes (CCNA2, CCNE2, E2F1 and CDK1) for further analysis (Supplementary Figure S8B).
	0.94	ASPM, CENPF, C15orf42, KIF4A, PBK, NUSAP1, HMMR, CIT, ANLN, SKA3, BIRC5, PRC1) and the 6-gene Panel B (CREB1/FoxA1 downregulated genes identified in abl cells: AZGP1, CRISPLD2, EPHX2, HSPB8, PTRF, MFGE8).
19790105	0.97	CITK is polarized to the ventricular surface where it interacts with the product of the human microcephaly-related gene ASPM at cytokinesis furrows and midbodies.
30214071	0.97	ASPM, WDR62, CEP152, MCPH1, CIT, CENPJ, and STIL.
22962576	0.96	ASPM, XRCC2, SPBC25, SMC4L1, SGOL1, SC65, PTTG1, POLE, PBK, MCM2, KNTC2, KIAA1794, EXO1, CIT, CHAF1B, CEP55, CDCA8, CDCA5, CDCA2, CDCA1, C20ort172, ANAPC11, CDC2, CDC20, CDC25C, CDC7, CDC27, and CDC25A (Table S1).
26871479	0.95	CIT, ASPM, SGOL2, KIF23, UBE21, TNKS and CCNB2), indicating the major impact of GPR160 on the G2/M phase of cell cycle.
31878213	0.93	MCPH5, MCPH17, MCPH20, and MCPH25) listed in Table 1 involve genes regulating the dynamic function of microtubules.
29375817	0.92	MCPH 17 (there are 17 genes identified so far that cause autosomal recessive primary microcephaly, MCPH arising from these 17 genes are termed from MCPH 1 to MCPH 17) and the majority of the genetic load in MCPH is contributed by the ASPM gene, making MPCH5 the most prevalent of all the types of MCPH.
29343805	0.88	ASPM and CIT as MCPH genes whose proteins localize to the midbody function.
29504900	0.76	ASPM, WDR62, CDK5RAP2, KNL1, CENPJ, STIL, CEP135, CEP152, CENPE, SASS6, CIT, and ANKLE2), while others are associated with chromosome condensation and maintenance (MCPH1, ZNF335, PHC1), cell cycle control (CDK6), and blood-brain barrier maintenance (MFSD2A).
21386884	0.55	CIT, ECT2, KIF23, PRC1, RACGAP1, ASPM, KIF18A and PLK1) contributes to the predictive power of the DM signature significantly more than the other genes.