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SNORD71 small nucleolar RNA, C/D box 71 [ Homo sapiens (human) ]

Gene ID: 692111, updated on 13-May-2022

Summary

Official Symbol
SNORD71provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 71provided by HGNC
Primary source
HGNC:HGNC:32732
See related
Ensembl:ENSG00000223224 AllianceGenome:HGNC:32732
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
MIRN768; HBII-239; hsa-mir-768
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Genomic context

See SNORD71 in Genome Data Viewer
Location:
16q22.2
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (71758402..71758487, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (77575597..77575682, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (71792305..71792390, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene PH domain and leucine rich repeat protein phosphatase 2 Neighboring gene Sharpr-MPRA regulatory region 2747 Neighboring gene uncharacterized LOC124903712 Neighboring gene small nucleolar RNA, H/ACA box 70D Neighboring gene adaptor related protein complex 1 subunit gamma 1 Neighboring gene parathymosin-like Neighboring gene uncharacterized LOC124903714

Genomic regions, transcripts, and products

Bibliography

General gene information

Other Names

  • microRNA 768

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_003059.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC010653
    Related
    ENST00000411292.1

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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    71758402..71758487 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    77575597..77575682 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)