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SNORA37 small nucleolar RNA, H/ACA box 37 [ Homo sapiens (human) ]

Gene ID: 677819, updated on 13-May-2022

Summary

Official Symbol
SNORA37provided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 37provided by HGNC
Primary source
HGNC:HGNC:32630
See related
Ensembl:ENSG00000207233 AllianceGenome:HGNC:32630
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
ACA37
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Genomic context

See SNORA37 in Genome Data Viewer
Location:
18q21.2
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (54222284..54222412, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (54425359..54425487, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (51748654..51748782, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904304 Neighboring gene ribosomal protein L29 pseudogene 32 Neighboring gene Sharpr-MPRA regulatory region 14779 Neighboring gene methyl-CpG binding domain protein 2 Neighboring gene uncharacterized LOC124904306 Neighboring gene uncharacterized LOC124904307 Neighboring gene DNA polymerase iota

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • ACA37 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_002970.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AJ609444
    Related
    ENST00000384504.1

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
    54222284..54222412 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    54425359..54425487 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)