RNA, U4atac small nuclear (U12-dependent splicing) is a small nuclear RNA that in humans that is encoded by the RNU4ATACgene.[1]
The small nuclear RNA (snRNA) encoded by this gene is part of the U12-dependent minor spliceosome complex. In addition to the encoded RNA, this ribonucleoprotein complex consists of U11, U12, U5, and U6atac snRNAs. The U12-dependent spliceosome acts on approximately 700 specific introns in the human genome. Defects in this gene are a cause of aka Taybi Linder syndrome or microcephalic osteodysplastic primordial dwarfism type 1 (MOPD1).[1]
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