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SNORD13H small nucleolar RNA, C/D box 13H [ Homo sapiens (human) ]

Gene ID: 109617018, updated on 10-Oct-2023

Summary

Official Symbol
SNORD13Hprovided by HGNC
Official Full Name
small nucleolar RNA, C/D box 13Hprovided by HGNC
Primary source
HGNC:HGNC:52247
See related
AllianceGenome:HGNC:52247
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 SNORD13H in Genome Data Viewer
Location:
16q22.1
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (69708572..69708675, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (75510754..75510857, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (69742475..69742578, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene ReSE screen-validated silencer GRCh37_chr16:69599594-69599770 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 7663 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 7664 Neighboring gene microRNA 1538 Neighboring gene nuclear factor of activated T cells 5 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11043 Neighboring gene MPRA-validated peak2631 silencer Neighboring gene ReSE screen-validated silencer GRCh37_chr16:69753551-69753732 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr16:69760025-69761224 Neighboring gene NAD(P)H quinone dehydrogenase 1 Neighboring gene NQO1 divergent transcript Neighboring gene NIN1 (RPN12) binding protein 1 homolog

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_145753.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC092115

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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    69708572..69708675 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    75510754..75510857 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)