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SNORA56 small nucleolar RNA, H/ACA box 56 [ Homo sapiens (human) ]

Gene ID: 677835, updated on 13-May-2022

Summary

Official Symbol
SNORA56provided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 56provided by HGNC
Primary source
HGNC:HGNC:32650
See related
Ensembl:ENSG00000206693 AllianceGenome:HGNC:32650
Gene type
snoRNA
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ACA56
Summary
Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residue U1664 of 28S rRNA. [provided by RefSeq, Feb 2009]
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Genomic context

See SNORA56 in Genome Data Viewer
Location:
Xq28
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (154774998..154775126)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (153011410..153011538)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (154003273..154003401)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene GRB2 associated binding protein 3 Neighboring gene Sharpr-MPRA regulatory region 12525 Neighboring gene small nucleolar RNA, H/ACA box 36A Neighboring gene dyskerin pseudouridine synthase 1 Neighboring gene microRNA 664b Neighboring gene MAGUK p55 scaffold protein 1 Neighboring gene high mobility group nucleosome binding domain 1 pseudogene 37

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • ACA56 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)

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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_002984.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AJ609449
    Related
    ENST00000383966.1

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    154774998..154775126
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    153011410..153011538
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)