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SNORD95 small nucleolar RNA, C/D box 95 [ Homo sapiens (human) ]

Gene ID: 619570, updated on 13-May-2022

Summary

Official Symbol
SNORD95provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 95provided by HGNC
Primary source
HGNC:HGNC:32757
See related
Ensembl:ENSG00000264549 AllianceGenome:HGNC:32757
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
U95
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Genomic context

See SNORD95 in Genome Data Viewer
Location:
5q35.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (181243314..181243376, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (181803266..181803328, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (180670314..180670376, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene tripartite motif containing 41 Neighboring gene receptor for activated C kinase 1 Neighboring gene small nucleolar RNA, C/D box 96A Neighboring gene uncharacterized LOC101928649 Neighboring gene tripartite motif containing 52 Neighboring gene TRIM52 antisense RNA 1 (head to head)

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • C/D box snoRNA U95

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_002591.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AY349594
    Related
    ENST00000579879.1

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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    181243314..181243376 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    181803266..181803328 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)