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SNORA21B small nucleolar RNA, H/ACA box 21B [ Homo sapiens (human) ]

Gene ID: 109617002, updated on 10-Dec-2024

Summary

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Official Symbol
SNORA21Bprovided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 21Bprovided by HGNC
Primary source
HGNC:HGNC:52195
See related
Ensembl:ENSG00000252699 AllianceGenome:HGNC:52195
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

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See SNORA21B in Genome Data Viewer
Location:
17q12
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (38851524..38851658, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (39714575..39714709, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (37007777..37007911, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene sperm microtubule associated protein 1 Neighboring gene uncharacterized LOC124903994 Neighboring gene ribosomal protein L23 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr17:37008921-37010120 Neighboring gene small nucleolar RNA, H/ACA box 21 Neighboring gene ribosomal protein S20 pseudogene 35

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. An updated human snoRNAome. Jorjani H, et al. Nucleic Acids Res, 2016 Jun 20. PMID 27174936, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

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_145761.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC110749
    Related
    ENST00000516890.1

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    38851524..38851658 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    39714575..39714709 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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