U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SNORD73B small nucleolar RNA, C/D box U73B [ Homo sapiens (human) ]

Gene ID: 114655, updated on 13-May-2022

Summary

Official Symbol
SNORD73Bprovided by HGNC
Official Full Name
small nucleolar RNA, C/D box U73Bprovided by HGNC
Primary source
HGNC:HGNC:30357
See related
Ensembl:ENSG00000201264 AllianceGenome:HGNC:30357
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
U73B; RNU73B
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See SNORD73B in Genome Data Viewer
Location:
4q31.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (151102057..151102131)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (154425941..154426015)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (152023209..152023283)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene LPS responsive beige-like anchor protein Neighboring gene LRBA intron ENCODE-defined enhancer Neighboring gene uncharacterized LOC107986196 Neighboring gene adenylate kinase 4 pseudogene 6 Neighboring gene Sharpr-MPRA regulatory region 3738 Neighboring gene small nucleolar RNA, C/D box 73A Neighboring gene ribosomal protein S3A Neighboring gene SH3 domain containing 19

Genomic regions, transcripts, and products

General gene information

Other Names

  • RNA, U73B small nucleolar pseudogene
  • U73B small nucleolar RNA
  • U73B snoRNA
  • small nucleolar RNA, C/D box U73B (pseudogene)

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_145963.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC095055
    Related
    ENST00000364394.1

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    151102057..151102131
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_025791772.1 Reference GRCh38.p14 PATCHES

    Range
    38788..38862
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    154425941..154426015
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_000961.3: Suppressed sequence

    Description
    NG_000961.3: This RefSeq was removed because it is now thought that this gene represents a functional snoRNA.