RNA, U4atac small nuclear 15, pseudogene (RNU4ATAC15P)

RNU4ATAC15P is a human pseudogene annotated as “RNA, U4atac small nuclear 15, pseudogene”. It is classified as a non-coding RNA pseudogene, meaning it resembles the functional U4atac snRNA gene (which is essential for the minor spliceosome complex and minor intron splicing) but lacks the capacity to produce a functional product. There is no evidence of transcriptional activity, protein coding, or association with biological functions, disease processes, or drug interactions. Unlike the functional RNU4ATAC gene, which is implicated in rare genetic syndromes through pathogenic variants[6], RNU4ATAC15P is not a therapeutic target, is not used clinically, and does not belong to a druggable molecular family. This entry is sometimes confused with the functional U4atac snRNA gene (*RNU4ATAC*), mutations in which are associated with developmental syndromes (Taybi-Linder/MOPD1, Roifman, Lowry-Wood)[6]. However, *RNU4ATAC15P* is strictly a pseudogene variant and lacks current biological or clinical relevance[1][5].

Other names

RNU4ATAC15PRNA, U4atac small nuclear 15, pseudogeneHGNC:46901

None (No therapeutic mechanism of action, as it is not a drug target[1][5].)