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MI0000234
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MIPF0000063
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GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC
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MIMAT0000222
hsa-miR-192-5p
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CUGACCUAUGAAUUGACAGCC
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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.
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MI0000234
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MIPF0000063
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GCCGAGACCGAGUGCACAGGGCUCUGACCUAUGAAUUGACAGCCAGUGCUCUCGUCUCCCCUCUGGCUGCCAAUUCCAUAGGUCACAGGUAUGUUCGCCUCAAUGCCAGC
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MIMAT0000222
hsa-miR-192-5p
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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.
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