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RNU2-22P RNA, U2 small nuclear 22, pseudogene [ Homo sapiens (human) ]

Gene ID: 106660611, updated on 23-Nov-2021

Summary

Official Symbol
RNU2-22Pprovided by HGNC
Official Full Name
RNA, U2 small nuclear 22, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48515
See related
Ensembl:ENSG00000223198
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See RNU2-22P in Genome Data Viewer
Location:
2q37.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (231501990..231502201, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (232366701..232366912, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene nucleolin Neighboring gene small nucleolar RNA, C/D box 82 Neighboring gene uncharacterized LOC107985998 Neighboring gene long intergenic non-protein coding RNA 471 Neighboring gene neuromedin U receptor 1

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_042900.1 

    Range
    101..312
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    231501990..231502201 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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