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SNORD33 small nucleolar RNA, C/D box 33 [ Homo sapiens (human) ]

Gene ID: 26818, updated on 13-May-2022

Summary

Official Symbol
SNORD33provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 33provided by HGNC
Primary source
HGNC:HGNC:10160
See related
Ensembl:ENSG00000199631 AllianceGenome:HGNC:10160
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
U33; RNU33
Summary
Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See SNORD33 in Genome Data Viewer
Location:
19q13.33
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (49490617..49490699)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (52490582..52490664)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (49993874..49993956)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene fms related receptor tyrosine kinase 3 ligand Neighboring gene ribosomal protein L13a Neighboring gene small nucleolar RNA, C/D box 32A Neighboring gene small nucleolar RNA, C/D box 34 Neighboring gene small nucleolar RNA, C/D box 35A

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • RNA, U33 small nucleolar
  • U33 small nucleolar RNA
  • U33 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_000020.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AB028893
    Related
    ENST00000362761.1

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_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    49490617..49490699
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    52490582..52490664
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)