Target intelligence / Profile preview

RNA, U2 small nuclear 2 (RNU2-2)

Target
RNU2-2
Molecular classification
Other, Small nuclear RNA (snRNA), Noncoding RNA, Component of ribonucleoprotein (snRNP)
01

Overview

RNA, U2 small nuclear 2 (RNU2-2) encodes a small nuclear RNA (snRNA) that is an essential RNA component of the spliceosome, the molecular machinery responsible for removing introns from precursor messenger RNA (pre-mRNA) in eukaryotes[1][4][7]. RNU2-2 is one of several gene loci encoding U2 snRNA in humans; unlike RNU2-1, RNU2-2 maps uniquely to chromosome 11 and was previously annotated as a pseudogene but is now known to be expressed and stably incorporated into the spliceosome[2][11][14]. U2 snRNA interacts with the intronic branch site and other snRNAs (notably U6) and critical proteins to orchestrate intron recognition and catalysis during splicing[1][4][7]. Mutations in RNU2-2 have been implicated in severe neurodevelopmental disorders with epilepsy, and recurrent somatic mutations affect multiple cancer types[2][8][11]. U2 snRNA is not a traditional drug target like receptors or enzymes but is a pivotal noncoding RNA, and its misregulation or mutation has clear disease implications[2][8][11]. No direct drug interactions are known, and it is excluded from standard target classes such as enzyme or receptor, falling instead under "Other" as a noncoding RNA and core spliceosomal component[1][4][7][14].

Other names
U2U2 small nuclear RNA 2U2 snRNA 2U2-2RNU2-2P (historic/pseudogene annotation)U2 spliceosomal RNA
02

Biological functions

Pre-mRNA splicingSpliceosome assemblyRecognition of branch point in intronsRegulation of gene expression
03

Disease associations

CancerNeurodevelopmental disorder (with prominent epilepsy)Other (general roles in spliceosome-related diseases)
04

Biomarkers

Mutations as potential biomarkers in specific cancers and neurodevelopmental disorders[2][8][11]

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