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SNORD116-1 small nucleolar RNA, C/D box 116-1 [ Homo sapiens (human) ]

Gene ID: 100033413, updated on 13-May-2022

Summary

Official Symbol
SNORD116-1provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 116-1provided by HGNC
Primary source
HGNC:HGNC:33067
See related
Ensembl:ENSG00000207063 MIM:605436; AllianceGenome:HGNC:33067
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
PWCR1; HBII-85-1
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Genomic context

See SNORD116-1 in Genome Data Viewer
Location:
15q11.2
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (25051476..25051572)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (22788135..22788231)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (25296623..25296719)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA host gene 14 Neighboring gene small nucleolar RNA, C/D box 109A Neighboring gene small nucleolar RNA, C/D box 116-2 Neighboring gene small nucleolar RNA, C/D box 116-3 Neighboring gene small nucleolar RNA, C/D box 116 cluster Neighboring gene Prader Willi/Angelman region RNA 6

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

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.

Genomic

  1. NG_002690.1 

    Range
    270567..270663
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. NR_003316.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC124312
    Related
    ENST00000384335.1

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_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    25051476..25051572
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    22788135..22788231
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)