We have generated a dot-bracket structure for each sequence using RNAfold.
Unambiguous secondary structure.
Parsed and ASCII art drawn.
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Caution, this is an AI generated summary based on literature. This may have errors. ?
MIR212 is a microRNA that has been studied for its effects on the proliferation and apoptosis of ovarian cancer (OC) cell lines [PMC6995389]. In a meta-analysis of Series 1 6 and 10-month data, as well as human BA9 data, eight microRNAs (Mir615, Mir135b, MIR212, Mir132, Mir20a, Mir708, Mir99a, Mir138-2) were found to be significantly associated with CAG length [PMC5764268]. These microRNAs passed the p-value threshold of 0.05 and had a false discovery rate (FDR) less than 0.05 [PMC5764268]. The specific role of MIR212 in this association was not mentioned in the given context. However, it is worth noting that MIR212 has been previously implicated in various biological processes and diseases. For example, it has been shown to be involved in the regulation of cell proliferation and apoptosis in different cancer types [PMC6995389]. Additionally, MIR212 has been associated with neurodegenerative diseases such as Alzheimer's disease [PMC5764268]. Further research is needed to fully understand the role of MIR212 in OC cell lines and its association with CAG length.
-- accccgcccgga c c -cA U CU C ccc c
cggggc cag gcg cgg CC UGGCU AGACUG UUACUg ggg
|||||| ||| ||| ||| || ||||| |||||| |||||| ||| c
gccccg guc cgc gcc GG ACUGA UCUGAC AAUgac ccc
cc ------------ - a aCC C CC - --u g
Annotation confidence
High
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This human miRNA was predicted by computational methods using conservation with mouse and Fugu rubripes sequences [1]. Expression of the excised miR has been validated in zebrafish, and the 5' end mapped by PCR. The 3' end was not experimentally determined. The sequence maps to human chromosome 17, but its expression has not been experimentally verified in human.