错误信息提示:
错误号:12142

错误原因:Table 'hscellor_ncrdeathdb.ncrnadeathmiRNA2targetDB' doesn't exist

错误sql语句:
select * from ncrnadeathmiRNA2targetDB where mirnaSymbol like '%miR-192' and taxid like '9606'
——错误记录被保存!

ncRNADetailInformation
  • Detail Information
  • Functional analysis
miRNA namepre-miRNA familypre-miRNA Sequencemature-miRNAmature sequencepre-miRNA description
miR-192
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0004543

hsa-miR-192-3p
CUGCCAAUUCCAUAGGUCACAG Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
MI0000234 MIPF0000063 GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC MIMAT0000222

hsa-miR-192-5p
CUGACCUAUGAAUUGACAGCC Lagos-Quintana et al. validated the presence of an 18 nt excised sequenceby cloning . Lim et al. predicted the miR by computational methodsusing conservation with mouse and Fugu rubripes sequences. Expression ofthe excised miR was validated in zebrafish, and the 5' end mapped by PCR. The 3' ends of the reported sequences differ by 3 nt - this entrycontains the longer sequence. Lim et al. report three separate copies ofthis gene named mir-192-1, -2 and -3 based on 2001 human genome assemblies. Subsequent assemblies suggest the presence of only one gene locatedon chromosome 11.
link to database TargetScanS 6.2 | MicroCosm | microRNA.org | miRNAMap 2.0
Interacted genes from RAID,miRTarBase
ZBTB10,CNTNAP3,RECK,RET,CCNO,CMTM6,HNF1B,CCNE1,ACTR2,PPP1CA,RNF26,USP34,RHOBTB3,RAD1,KLHL23
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ZBTB10,CNTNAP3,RECK,RET,CCNO,CMTM6,HNF1B,CCNE1,ACTR2,PPP1CA,RNF26,USP34,RHOBTB3,RAD1,KLHL23,VGLL3,UPP1,KIF15,RPAP2,SLC9A5,NOD2,CAB39L,INPP5F,KLHDC5,RNASEL,VASH2,LRRFIP1,EPM2AIP1,CLSPN,KAT2B,CCZ1,RAB23,PIK3R4,NMU,GPSM2,MT1X,PARN,ATG4A,RNFT1,CADPS2,USP1,ZMYM1,SAMD3,MYB,IL7,IFRD1,KIF20B,NPHP3,XK,RAB27A,IL1R1,DYRK1A,ZNF263,SGMS2,RUFY3,CCDC7,TFCP2L1,PET112,FNBP1,PAFAH1B1,C5orf30,LARP1B,ST3GAL6,MCM9,SLC19A2,RPGRIP1L,CD164,LMNB1,TMEFF1,NCAPH,ZNF226,SNX10,DENND1A,FEN1,CCDC15,FZD1,ERMP1,LIMS1,SERAC1,RAB40B,RAB1A,NUDT15,ASPH,XPO1,PDLIM3,CCDC14,SLC35F3,RPS6KB1,SLC25A30,C18orf54,THBD,UVRAG,HSP90B1,FAM189A2,MPZL1,AHSA2,HBXIP,CTNNBIP1,HMGCS1,FAM20B,NAA50,NRG4,FBXO25,CCL3L1,MED22,TRIM23,RAB8B,CXorf57,RSBN1,CCDC150,FKBP15,NCBP1,RAB11FIP2,ITGAV,CMPK2,CDKN3,CYP24A1,ARFGEF1,STX7,FANCI,ALG10,PRNP,PLS3,NPNT,IL6ST,PASK,ZFP161,MTSS1,C21orf91,PPARG,HOOK3,CKAP2L,AFAP1L1,EAF2,ODC1,KDM4D,USP45,TMEM164,C3orf19,KCNMB4,KHDRBS3,INSIG1,FUBP1,HJURP,CLK1,CENPF,ZNF215,GNRH1,XPA,PIM1,CKAP4,KRT18P8,PITPNC1,IMPA1,BTNL9,TICAM2,ZNF320,BCL2L13,ZNF611,APPL1,GPR19,IL28RA,TRIM59,UBIAD1,ZNF652,HIBADH,RAD21,ID1,SLC48A1,TOR1AIP1,C9orf125,RADIL,STIL,MRPL50,ANKRD13A,IDI1,WDR44,ZDHHC23,EFCAB11,PLK4,TARDBP,LMAN1,MMAB,TCAM1P,C1orf96,LEPROTL1,NEDD1,DNAJC19,NHSL1,DSTYK,FERMT1,MCM10,BMPR2,EIF2C2,C4orf32,ERCC6L,SEC63,PARM1,DNAJB9,WDR67,CUL5,LYPD6,SPARC,PGM3,CCDC18,GPC4,SLC35G1,PRICKLE1,NEK1,LMNB2,FBN1,NEIL3,ZBTB33,EXTL2,FAM171B,VANGL1,AP3M2,C1orf198,GABPB2,TMEM17,PAK6,ZNF823,AGPAT5,ZFYVE28,C1orf53,ZNF200,KCNS3,FBXW2,HYLS1,PPM1A,SLC26A2,ZNF238,CSGALNACT2,PCSK9,KLF10,PRIM1,C6orf72,HSPBAP1,LRIG1,NFKBIZ,SPRY4,RNASE4,ANKRD32,ZMAT3,RECQL,DHCR24,RRM1,FAM136A,SEC23B,SLC7A11,ZDHHC2,TTK,TRAPPC2P1,C20orf11,PPP2R3B,KIAA1143,PRSS23,TOPBP1,ELL2,EMB,DGCR11,ZNF780A,WHSC1,NFIB,PHF6,ZNF273,CUZD1,SCRN3,FAM83D,BIVM,DIMT1,ZBTB34,MSN,CDKN2A,RNPC3,DLGAP5,C2orf49,RANBP3,NAB1,EPM2A,RABGAP1,CMPK1,MAP6D1,UBE2D1,GATM,GAB2,SAP30,CLSTN1,SATB2,BUB1B,ATP1B1,ALCAM,ATP10D,FZD7,RSBN1L,C3orf64,DSN1,DDOST,CERS6,ZNF704,WDR47,SRD5A1,PRKAR1A,DEPDC1,CENPI,EPS8,KIF5C,NDFIP2,OPA1,RBL2,SFR1,RFWD3,RASSF8,FAM63B,GOLGA6A,BTF3L4,TTPA,MSH6,B4GALT6,STAMBPL1,BRD3,PAPD7,TCFL5,OTUD3,GPR137C,MACF1,FOS,CGNL1,C17orf58,DDX50,ACADSB,DEGS1,PURA,L2HGDH,POLA2,UBL3,PIGM,UGT8,ACSL1,LRRC58,ERCC3,MTDH,ARL2BP,PTP4A3,MPP5,ABCB10,LEAP2,SEPT10,LRRC8C,MAP1LC3B,TRIM68,DST,TCHP,CEP78,IRAK4,UQCRC2,TRPC1,NUCKS1,TOP1P2,IL1RAP,CEP128,LARS,DEAF1,CENPA,KPNA5,TMEM2,USP18,PITPNB,LIPA,MAN2A2,BRWD1,COPS7A,ZNF443,ZNF165,EME1,ZSWIM3,CHPT1,MRPL13,PPP1R12A,NOB1,FBXO4,ABCG2,SCD,DTL,RNF141,B3GALNT1,STK3,LIMCH1,AKAP11,TPGS2,ASRGL1,PPAT,DEK,PRRC1,SLC46A3,C5orf34,PIP4K2B,BICD1,KLHL15,TMEM30A,SH3BP4,C14orf45,TBL1X,TRPV1,OSBPL6,E2F5,ESCO2,UCK1,COBLL1,GSG2,ORC1,SAYSD1,KIF14,SPTBN1,REEP1,TBC1D22B,ACVR2A,ALG10B,NUFIP1,SOAT1,SYNGR1,POU2F1,CADM1,TMTC2,PHF17,TMEM169,ALDH5A1,TOR1B,PSMD6,KDELC2,CIT,SOWAHC,TNFSF13B,PAWR,RBP7,KLHL8,PANX1,KIF5B,ZNF248,ANG,LHFP,TOP1,ARNTL2,ELOVL5,FGF2,GATAD1,SCMH1,KIF24,PDE2A,ENDOD1,C2orf44,CASP7,UACA,FAM178A,FGFR1OP,MMP20,DNAJC3,XIAP,RAB2A,ELOVL1,C10orf137,CA8,BARD1,MIS12,PABPC4,EPDR1,PCDH7,PPP1R26,SNRPD1,MANF,USP14,SENP1,SMARCA2,MEIS2,SERTAD4,AP1S2,MRPL43,PLCE1,KIAA0240,MSRB3,HINT3,NIPAL1,SMC2,LOXL2,CDON,CA13,STXBP4,PLEKHF2,DDX3X,BRCA2,CRK,ANKRD6,WNT3,LSM14B,E2F8,SBDSP1,HERC2,STOX2,TMTC3,C8orf47,SH2B3,TJP2,GRIA1,WNK1,KIAA1671,ZIC5,MAPK9,C8orf46,COQ3,AGL,FADS1,LHFPL4,CDC25A,KIF20A,ZMYND11,UHRF1BP1,HAUS3,VPS13C,NCOA3,SEMA4D,RAD51,C13orf27,NDE1,DDX54,ARHGAP11A,TNFSF13,BTC,GALNT12,LRRCC1,EIF2AK3,NUF2,CREBL2,APC,ZNF267,EEA1,STAM,ZNF385B,PRKD3,TDG,TMEM194A,RTKN2,TMEM136,IQCC,CLN6,CDKN2D,CPSF6,PERP,C15orf24,ATP6V1G1,ENPP4,PSRC1,C6orf168,C1D,FAM111B,FZD4,ARHGEF10,ECT2,RNF6,RDM1,MAD2L1,PTPLAD1,C11orf51,GEN1,HOXB9,LRP8,MCM3,NKX3-1,C1QTNF3,ID2,NUCB2,RP9P,ARHGEF40,MIS18BP1,RSRC1,ABCA8,HOXA10,FBXO3,PHTF2,RCC2,IRAK1,GAS2L3,PRDM4,DCP1A,EHBP1L1,ZNF230,NPTXR,SGCB,HCN3,MAP3K1,DDHD1,ZNF184,KIAA1731,MTMR12,FAM126B,FANCM,SKA1,CFL2,TRIB3,KIF18A,PXDN,ZFP30,WDR76,CENPE,CASC5,CORO2B,THOP1,FOXA1,TRAF3IP3,FAM199X,FHDC1,NLK,C5orf13,ZFP1,LIN9,DLG5,ARHGAP19,ZNF85,USP12,PIGX,TMPO,PCGF5,ZXDC,KATNAL1,C12orf65,CENPK,BRCA1,ANLN,FLVCR1,RAB6C,CDCA4,NFYA,DHFRL1,ZNF45,PXDC1,GLCCI1,PLEKHG2,PRKAA2,MCM6,UBASH3B,C16orf52,FNDC3B,HES6,CTCF,RACGAP1,ERCC4,CRLF3,MIB1,KIAA1958,RB1,IGF1R,SPIN4,PTS,MTERFD1,CHSY3,COCH,SPATA13,TMTC4,C9orf80,MEX3B,TCF7,C10orf35,G2E3,ATXN7,SPAG9,SYNCRIP,OGFRL1,PRPS2,ENTPD3,NIPA1,CHDH,AKAP9,CREBZF,FAM120AOS,SLC7A2,HCN4,ZADH2,KBTBD11,TMC3,B3GNT5,CDK14,CHML,METTL9,C8orf55,MT1F,TMEM200A,CTH,SLC39A9,SIRT1,HESX1,BGLAP,CDC20,KDM1B,FBXO36,ENC1,ACSF3,APOLD1,UBE2V2,CEP55,ZBTB6,TMEM188,ZNF701,HIATL1,PRPF38A,PHF19,C12orf34,NKRF,ZNF346,RMI1,SLC1A4,SGOL2,SLC35B4,TTF2,DNAL1,FBXO31,FAIM,IGDCC4,RPAP3,HMMR,FAM71E1,TPM4,BORA,CD83,LYSMD3,NMI,CLIP4,EIF2S1,C9orf163,FAM126A,SPCS3,MIPOL1,DIS3L,DNAJB4,CIB2,MDM4,ID4,NHLRC3,FAM101B,NBN,ATRNL1,FAM132B,PRADC1,TFG,FUT11,RNF219,LOC81691,CLVS1,TCEB3,MKI67,PIF1,ACVR2B,ARHGEF26,SGPP1,TMED10,ENTPD7,FAM110C,ITGB1,TMEM66,EFNB2,EGR1,ATAD1,TMEM180,KIF23,CCDC47,PRRG4,BMP2K,SLC16A6,MCART1,CLK4,SAMD13,ZC3H12C,TUBGCP3,PHF10,KIAA1841,MFI2,ANO6,ICAM3,LYRM7,KIDINS220,NSF,GCH1,C6orf62,HBEGF,CKLF,BRIP1,IQGAP1,IRX4,KCTD12,BBS7,MNS1,DBF4B,MOAP1,CHD7,PHC2,PLAU,CDKN1B,ENOSF1,LGMN,RFC4,CUL3,SP4,DCBLD2,NIN,ZNF641,ZNF519,TRAIP,PPP1CB,HS3ST3B1,ZEB2,POLQ,PKP4,MXI1,SLC16A14,C1orf112,ARL4C,GPR180,BLM,SIX4,CEP19,CHM,CHST12,CCNY,NT5M,SMC4,ATP5L,SETD4,OSBPL10,HADH,RCBTB2,CCZ1B,SLC25A40,DICER1,AMMECR1,UNG,BYSL,PLOD1,BCOR,SLCO3A1,SMARCB1,AASDHPPT,BCORL1,GRHL1,AKAP7,PHTF1,ANAPC10,USP54,PCOLCE2,CCDC121,PTPRE,TRIP13,TDP1,SLC16A7,STK17B,ADRBK2,EML1,TAF9B,ZNF114,MKL2,ATG10,ABCC3,KIAA0090,ARHGAP29,CCDC111,SASS6,RAP1GAP,HOXA13,ROPN1L,ZNHIT3,ACTR1B,LRRFIP2,SEC24D,RIMKLA,CYP4V2,CAMK4,EAF1,GPR126,OTUD1,ZNF449,MCAM,C15orf42,CTPS2,BCL2,NCEH1,N4BP2,NOXO1,ALDH9A1,PODXL,ERLIN2,TROAP,ATAD5,PAPD5,NAA20,DNAJB5,IL15,UBE2W,PLAGL2,WHSC1L1,SLC39A1,SS18,KCTD15,TMEM106A,CLIC1,GULP1,WWC2,HSPA2,ZNF525,PTBP2,SLC39A8,C16orf46,RAD54B,LMLN,DUSP16,C1orf86,OVOL1,PPP2R2D,TOR3A,RIC8B,MFSD10,FBXO5,IL17RB,PARP16,SNX13,ATF1,ICK,HAS3,CDC7,EEF1A2,SAMHD1,DBT,WWC3,RAB3B,ASPM,PSMC3IP,MBNL3,GPR37,FAM59B,TIFA,ATAD2,OSBPL8,UBE2D2,OTUB2,NCBP2,CDC14A
KEGG pathways enriched for interacted genes
pathway namepathway descriptiontarget genes enrich in pathwayp-value
hsa04110 Cell cycle MCM3,MCM6,CDC14A,CDC7,CDKN2A,E2F5,RB1,CDKN1B,CDKN2D,ORC1,ANAPC10,CDC25A,CDC20,RBL2,RAD21,BUB1B,TTK,CCNE1,MAD2L1, 4.17E-5
hsa05200 Pathways in cancer TFG,APPL1,CDKN2A,CDKN1B,XIAP,WNT3,NKX3-1,IGF1R,FZD1,FZD4,FGF2,FZD7,RAD51,MSH6,HSP90B1,MAPK9,BRCA2,BCL2,APC,RB1,PPARG,CRK,ITGAV,RET,ITGB1,TCF7,FOS,CCNE1, 6.65E-2
hsa05210 Colorectal cancer MAPK9,IGF1R,FZD1,FZD4,BCL2,FZD7,APPL1,TCF7,MSH6,APC,FOS, 8.76E-2
hsa03440 Homologous recombination BRCA2,NBN,EME1,RAD51,RAD54B,BLM, 1.16E-1
hsa03030 DNA replication MCM3,MCM6,POLA2,FEN1,RFC4,PRIM1, 3.21E-1
Gene ontology terms enriched for interacted genes
GO termsGO terms descriptiontarget genes enrich in GO termp-value
GO:0007049 cell cycle RACGAP1,CDC7,PSMD6,SBDSP1,OVOL1,CREBL2,MSH6,MIS12,KIF15,BRCA2,FBXO31,MDM4,BRCA1,GSG2,RAD54B,DSN1,CUZD1,DHCR24,ITGB1,DBF4B,NDE1,ERCC6L,ID4,RBL2,FANCI,RCC2,RABGAP1,FAM83D,CDC14A,NCAPH,APPL1,PAFAH1B1,SASS6,CEP55,ESCO2,LIN9,LRRCC1,PSRC1,MCM3,MCM6,BCL2,KAT2B,SMC2,HAUS3,APC,CENPF,FBXO5,CENPE,MACF1,UBE2D1,CENPA,TARDBP,NUF2,CDC25A,CDC20,RAD1,SGOL2,CCNE1,PAPD5,CLSPN,SKA1,SMARCB1,BLM,ANAPC10,KIF23,PSMC3IP,RAD51,BUB1B,RAD21,ASPM,HSPA2,BARD1,CUL5,RB1,BGLAP,NEDD1,KIF20B,MNS1,CUL3,NEK1,PPP1CB,PPP1CA,PPP2R3B,DLGAP5,LMLN,MIS18BP1,MAD2L1,PAPD7,SMC4,TRIP13,SH3BP4,NBN,CDKN2A,CDKN1B,SEPT10,BORA,DST,CDKN2D,CDKN3,HJURP,TTK,ZMYND11,E2F8,KIF18A,CIT,ANLN,PIM1,MKI67,GAS2L3, 3.20E-22
GO:0022403 cell cycle phase SKA1,CDC7,BLM,ANAPC10,OVOL1,KIF23,PSMC3IP,MSH6,RAD51,BUB1B,RAD21,ASPM,MIS12,KIF15,HSPA2,BRCA2,CUL5,RB1,BGLAP,RAD54B,DSN1,ITGB1,NEDD1,KIF20B,NEK1,MNS1,CUL3,PPP1CB,NDE1,PPP2R3B,ERCC6L,ID4,DLGAP5,MAD2L1,MIS18BP1,LMLN,PAPD7,SMC4,RCC2,TRIP13,FAM83D,NCAPH,NBN,PAFAH1B1,CDKN2A,CDKN1B,BORA,CDKN2D,CDKN3,CEP55,TTK,LRRCC1,BCL2,KIF18A,HAUS3,SMC2,APC,CENPF,FBXO5,CENPE,CIT,ANLN,PIM1,CDC25A,TARDBP,NUF2,MKI67,CDC20,RAD1,SGOL2,CCNE1,PAPD5, 8.85E-20
GO:0022402 cell cycle process SKA1,RACGAP1,CDC7,PSMD6,SBDSP1,BLM,ANAPC10,OVOL1,KIF23,PSMC3IP,MSH6,RAD51,BUB1B,RAD21,ASPM,MIS12,KIF15,BRCA2,HSPA2,BARD1,MDM4,BRCA1,CUL5,RB1,BGLAP,RAD54B,DSN1,DHCR24,ITGB1,NEDD1,KIF20B,NEK1,MNS1,CUL3,PPP1CB,NDE1,PPP2R3B,ERCC6L,ID4,DLGAP5,MAD2L1,MIS18BP1,LMLN,PAPD7,SMC4,RCC2,TRIP13,FAM83D,NCAPH,NBN,PAFAH1B1,CDKN2A,CDKN1B,SASS6,BORA,DST,CDKN2D,CDKN3,CEP55,TTK,LRRCC1,BCL2,KAT2B,SMC2,KIF18A,HAUS3,APC,CENPF,FBXO5,CENPE,CIT,ANLN,MACF1,UBE2D1,PIM1,CENPA,TARDBP,NUF2,CDC25A,MKI67,CDC20,RAD1,SGOL2,GAS2L3,CCNE1,PAPD5, 1.00E-19
GO:0000278 mitotic cell cycle SKA1,CDC7,PSMD6,BLM,ANAPC10,KIF23,BUB1B,RAD21,MIS12,ASPM,KIF15,CUL5,RB1,BGLAP,DSN1,ITGB1,NEDD1,KIF20B,CUL3,NEK1,NDE1,PPP2R3B,PPP1CB,ERCC6L,ID4,DLGAP5,MAD2L1,MIS18BP1,LMLN,PAPD7,SMC4,RCC2,FAM83D,NCAPH,PAFAH1B1,CDKN2A,CDKN1B,BORA,CDKN2D,CDKN3,CEP55,TTK,LRRCC1,BCL2,HAUS3,KIF18A,SMC2,APC,CENPF,CENPE,FBXO5,CIT,ANLN,UBE2D1,PIM1,CENPA,CDC25A,TARDBP,NUF2,CDC20,CCNE1,PAPD5, 3.77E-16
GO:0000279 M phase SKA1,ANAPC10,OVOL1,KIF23,PSMC3IP,MSH6,RAD51,BUB1B,RAD21,MIS12,ASPM,KIF15,HSPA2,BRCA2,RB1,BGLAP,RAD54B,DSN1,NEDD1,KIF20B,MNS1,NEK1,NDE1,ERCC6L,DLGAP5,MAD2L1,MIS18BP1,LMLN,PAPD7,SMC4,RCC2,TRIP13,FAM83D,NCAPH,NBN,PAFAH1B1,BORA,CEP55,TTK,LRRCC1,HAUS3,KIF18A,SMC2,APC,CENPF,CENPE,FBXO5,CIT,ANLN,CDC25A,TARDBP,NUF2,MKI67,RAD1,CDC20,SGOL2,PAPD5, 1.45E-15
KEGG pathways and Gene Ontology terms enriched for the interacted genes of ncRNA from RAID and miRTarBase.
disease namerelated genesp-value