U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SNORA22 small nucleolar RNA, H/ACA box 22 [ Homo sapiens (human) ]

Gene ID: 677807, updated on 13-May-2022

Summary

Official Symbol
SNORA22provided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 22provided by HGNC
Primary source
HGNC:HGNC:32612
See related
Ensembl:ENSG00000206634 AllianceGenome:HGNC:32612
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
ACA22; SNORA22A
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See SNORA22 in Genome Data Viewer
Location:
7q11.21
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (65755526..65755659)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (66977656..66977789)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (65220513..65220646)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene glutamate metabotropic receptor 8 pseudogene Neighboring gene long intergenic non-protein coding RNA 3006 Neighboring gene integrator complex subunit 4 pseudogene 2 Neighboring gene Sharpr-MPRA regulatory region 6763 Neighboring gene small nucleolar RNA, H/ACA box 15B-2 Neighboring gene chaperonin containing TCP1 subunit 6 pseudogene 1 Neighboring gene general transcription factor IIi pseudogene 5

Genomic regions, transcripts, and products

General gene information

Other Names

  • ACA22 snoRNA

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)

NEW Try the new Transcript table

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_002961.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AJ609437
    Related
    ENST00000383907.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    65755526..65755659
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    66977656..66977789
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)