MicroRNA 6132 (MIR6132)

MicroRNA 6132 (MIR6132) is a human gene belonging to the microRNA family of non-coding RNAs; these are short (typically 20–24 nucleotides) RNA molecules involved in the post-transcriptional regulation of gene expression by binding to target messenger RNAs (mRNAs), leading to either inhibition of translation or mRNA degradation[2][5][6]. MIR6132 is cataloged under HGNC:50272 and NCBI Gene:102466616[2]. Diseases associated with MIR6132 include Alopecia-Intellectual Disability Syndrome 1, but its specific biological role, regulated targets, or therapeutic relevance remain poorly characterized in the current literature[2]. If further specificity or functional insight emerges in curated databases or new literature, the above may be updated. At present, MIR6132 is recognized as a distinct human microRNA gene with very limited functional annotation.

Other names

hsa-mir-6132microRNA mir-6132MIR6132miR-6132