RNU2-2

RNU2-2 is a snRNA gene that encodes one of the functional homologs of U2 spliceosomal RNA. RNU2-2 was previously thought to be a pseudogene,^[2] but it has been shown to be functional.^[3] Specific heterozygous variants in RNU2-2 cause an autosomal dominant developmental and epileptic encephalopathy, also called RNU2-2 syndrome.^[4]

RNU2-2P
Identifiers
Aliases	RNU2-2P, RNU2-2, RNU2B, U2, RNA, U2 small nuclear 2, pseudogene
External IDs	GeneCards: RNU2-2P; OMA:RNU2-2P - orthologs
Orthologs Species Human Mouse Entrez 26855 n/a Ensembl ENSG00000222328 n/a UniProt n a n/a RefSeq (mRNA) n/a n/a RefSeq (protein) n/a n/a Location (UCSC) n/a n/a PubMed search [1] n/a
Wikidata
View/Edit Human