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SNORD113-2 small nucleolar RNA, C/D box 113-2 [ Homo sapiens (human) ]

Gene ID: 767562, updated on 10-Oct-2023

Summary

Official Symbol
SNORD113-2provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 113-2provided by HGNC
Primary source
HGNC:HGNC:32981
See related
Ensembl:ENSG00000212384 AllianceGenome:HGNC:32981
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
14q(I-2)
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Genomic context

See SNORD113-2 in Genome Data Viewer
Location:
14q32.31
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (100927342..100927412)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (95162771..95162841)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (101393679..101393749)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene maternally expressed 8, small nucleolar RNA host gene Neighboring gene microRNA 370 Neighboring gene small nucleolar RNA, C/D box 113-1 Neighboring gene small nucleolar RNA, C/D box 113-3 Neighboring gene small nucleolar RNA, C/D box 113-4

Genomic regions, transcripts, and products

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_003230.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL132709
    Related
    ENST00000391082.1

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_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    100927342..100927412
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    95162771..95162841
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)