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SNORD22 small nucleolar RNA, C/D box 22 [ Homo sapiens (human) ]

Gene ID: 9304, updated on 23-Nov-2021

Summary

Official Symbol
SNORD22provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 22provided by HGNC
Primary source
HGNC:HGNC:10145
See related
Ensembl:ENSG00000277194 MIM:603223
Gene type
snoRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
U22; RNU22
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Genomic context

See SNORD22 in Genome Data Viewer
Location:
11q12.3
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (62852910..62853035, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (62620382..62620507, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene STX5 divergent transcript Neighboring gene testis expressed 54 Neighboring gene WD repeat domain 74 Neighboring gene RNA, U2 small nuclear 2, pseudogene Neighboring gene small nucleolar RNA host gene 1 Neighboring gene small nucleolar RNA, C/D box 31 Neighboring gene small nucleolar RNA, C/D box 30

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • RNA, U22 small nucleolar

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in RNA processing IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in nucleolus IEA
Inferred from Electronic Annotation
more info
 

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.

RNA

  1. NR_000008.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AP001160
    Related
    ENST00000384756.1

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_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    62852910..62853035 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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