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SNORD31B small nucleolar RNA, C/D box 31B [ Homo sapiens (human) ]

Gene ID: 109616978, updated on 10-Oct-2023

Summary

Official Symbol
SNORD31Bprovided by HGNC
Official Full Name
small nucleolar RNA, C/D box 31Bprovided by HGNC
Primary source
HGNC:HGNC:52226
See related
Ensembl:ENSG00000201847 AllianceGenome:HGNC:52226
Gene type
snoRNA
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See SNORD31B in Genome Data Viewer
Location:
13q33.3
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (107320895..107320963, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (106546852..106546920, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (107973243..107973311, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene translation initiation factor IF-2-like Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:107569875-107570752 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:107638300-107638890 Neighboring gene uncharacterized LOC124903205 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:107844570-107845144 Neighboring gene NALCN channel auxiliary factor 1 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:107911110-107912309 Neighboring gene Sharpr-MPRA regulatory region 7214 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:108110377-108110878 Neighboring gene uncharacterized LOC105370353 Neighboring gene uncharacterized LOC112268110 Neighboring gene microRNA 1267

Genomic regions, transcripts, and products

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.

RNA

  1. NR_145739.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AL138914
    Related
    ENST00000364977.1

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    107320895..107320963 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    106546852..106546920 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)