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SNORD97 small nucleolar RNA, C/D box 97 [ Homo sapiens (human) ]

Gene ID: 692223, updated on 13-May-2022

Summary

Official Symbol
SNORD97provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 97provided by HGNC
Primary source
HGNC:HGNC:32760
See related
Ensembl:ENSG00000238622 AllianceGenome:HGNC:32760
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
U97
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Genomic context

See SNORD97 in Genome Data Viewer
Location:
11p15.4
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (10801467..10801608, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (10886369..10886510, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (10823014..10823155, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene inositol 1,4,5-triphosphate receptor associated 1 Neighboring gene Sharpr-MPRA regulatory regions 8950 and 14430 Neighboring gene CTR9 homolog, Paf1/RNA polymerase II complex component Neighboring gene uncharacterized LOC101928053 Neighboring gene eukaryotic translation initiation factor 4 gamma 2 Neighboring gene zinc finger BED-type containing 5

Genomic regions, transcripts, and products

General gene information

Markers

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_004403.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AY349597
    Related
    ENST00000459187.1

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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    10801467..10801608 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    10886369..10886510 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)