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SNORD4B small nucleolar RNA, C/D box 4B [ Homo sapiens (human) ]

Gene ID: 26772, updated on 13-May-2022

Summary

Official Symbol
SNORD4Bprovided by HGNC
Official Full Name
small nucleolar RNA, C/D box 4Bprovided by HGNC
Primary source
HGNC:HGNC:10098
See related
Ensembl:ENSG00000238597 AllianceGenome:HGNC:10098
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
Z17B; RNU101B
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Genomic context

See SNORD4B in Genome Data Viewer
Location:
17q11.2
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (28723681..28723754)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (29666488..29666561)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (27050699..27050772)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein L23a Neighboring gene small nucleolar RNA, C/D box 4A Neighboring gene small nucleolar RNA, C/D box 42A Neighboring gene TLC domain containing 1 Neighboring gene NIMA related kinase 8 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:27070105-27071105

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • RNA, U101B small nucleolar
  • U101B small nucleolar RNA
  • U101B snoRNA
  • Z17B small nucleolar RNA
  • Z17B snoRNA

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_000009.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AF001689
    Related
    ENST00000459083.1

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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    28723681..28723754
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    29666488..29666561
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)