Target intelligence / Profile preview

RNA U6 small nuclear 14, pseudogene (RNU6-14P)

Target
RNU6-14P
Molecular classification
Other (pseudogene, small nuclear RNA pseudogene)
01

Overview

RNU6-14P stands for "RNA U6 small nuclear 14, pseudogene". It is annotated as a pseudogene related to the U6 small nuclear RNA (snRNA) family, specifically the 14th member of these pseudogenes. U6 snRNA genes code for the RNA component of the spliceosome, a nuclear complex essential for pre-mRNA splicing[1][3][4].\nHowever, RNU6-14P is a **pseudogene**, meaning it does not produce a functional RNA and is generally considered non-coding and non-functional. Pseudogenes like RNU6-14P are the result of retrotransposition or genomic duplication followed by loss of function. They are not considered therapeutic targets, are not druggable, and have no biomarker utility or direct disease association[3].\nThe **canonical, functional version** of this molecule would be the U6 small nuclear RNA (RNU6-1 or related functional U6 genes), which play an essential role as part of the major spliceosome in splicing pre-mRNA[1][4]. Pseudogenes like RNU6-14P are not the active RNAs, do not perform a biological function, and are not targets for therapy or diagnostics.\nIf you are interested in a therapeutic target, the relevant entity would be the U6 small nuclear RNA, not the RNU6-14P pseudogene.\n\n- **Canonical references for U6 snRNA function:**\n - U6 snRNA is a central component in spliceosome assembly and catalysis, coordinating magnesium ions and positioning pre-mRNA for splicing reactions[1][4].\n - Pseudogenes such as RNU6-14P are numerous throughout the genome; they are markers of genome evolution and retrotransposition but lack function[3].

Other names
RNU6-14RNU6-14P
02

Mechanism of action

None

03

Biological functions

None (no known function; pseudogene of a spliceosomal RNA)
04

Disease associations

None (pseudogene; not implicated directly in disease)
05

Safety considerations

None
06

Interacting drugs

None
07

Biomarkers

None

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