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SNORD38A small nucleolar RNA, C/D box 38A [ Homo sapiens (human) ]

Gene ID: 94162, updated on 13-May-2022

Summary

Official Symbol
SNORD38Aprovided by HGNC
Official Full Name
small nucleolar RNA, C/D box 38Aprovided by HGNC
Primary source
HGNC:HGNC:30355
See related
Ensembl:ENSG00000202031 AllianceGenome:HGNC:30355
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
U38A; RNU38A
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Genomic context

See SNORD38A in Genome Data Viewer
Location:
1p34.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (44777842..44777912)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (44648831..44648901)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (45243514..45243584)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein S8 Neighboring gene small nucleolar RNA, C/D box 55 Neighboring gene small nucleolar RNA, C/D box 46 Neighboring gene small nucleolar RNA, C/D box 38B Neighboring gene ribosomal protein S15a pseudogene 11

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • RNA, U38A small nucleolar
  • U38A small nucleolar RNA
  • U38A 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_001456.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    X67247
    Related
    ENST00000365161.1

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    44777842..44777912
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    44648831..44648901
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)