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SNORD58A small nucleolar RNA, C/D box 58A [ Homo sapiens (human) ]

Gene ID: 26791, updated on 13-May-2022

Summary

Official Symbol
SNORD58Aprovided by HGNC
Official Full Name
small nucleolar RNA, C/D box 58Aprovided by HGNC
Primary source
HGNC:HGNC:10208
See related
Ensembl:ENSG00000206602 AllianceGenome:HGNC:10208
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
U58a; RNU58A
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Genomic context

See SNORD58A in Genome Data Viewer
Location:
18q21.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (49491283..49491347, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (49689024..49689088, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (47017653..47017717, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene RPL17-C18orf32 readthrough Neighboring gene microRNA 1539 Neighboring gene ribosomal protein L17 Neighboring gene small nucleolar RNA, C/D box 58C Neighboring gene small nucleolar RNA, C/D box 58B Neighboring gene signal recognition particle 72 pseudogene 1

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • RNA, U58A small nuclear

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_002571.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    X96657
    Related
    ENST00000383875.1

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_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    49491283..49491347 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    49689024..49689088 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)