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SNORD61 small nucleolar RNA, C/D box 61 [ Homo sapiens (human) ]

Gene ID: 26787, updated on 13-May-2022

Summary

Official Symbol
SNORD61provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 61provided by HGNC
Primary source
HGNC:HGNC:10218
See related
Ensembl:ENSG00000206979 AllianceGenome:HGNC:10218
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
U61; RNU61; HBII-342
Summary
Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box C/D class snoRNAs are involved in site-specific 2-prime-O-ribose methylation of preribosomal RNA precursors. This snoRNA is located in an intron of the RNA binding motif protein, X-linked gene (RBMX). [provided by RefSeq, Sep 2009]
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Genomic context

See SNORD61 in Genome Data Viewer
Location:
Xq26.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (136879199..136879271, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (135187926..135187998, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (135961358..135961430, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene RAN pseudogene 4 Neighboring gene RAB28, member RAS oncogene family pseudogene 5 Neighboring gene RNA binding motif protein X-linked Neighboring gene ribosomal protein L22 pseudogene 23 Neighboring gene transmembrane 9 superfamily member 5, pseudogene Neighboring gene serine/arginine repetitive matrix 1 pseudogene 3

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • RNA, U61 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_002735.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    X96661
    Related
    ENST00000384252.1

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    136879199..136879271 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    135187926..135187998 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)