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SNORD8 small nucleolar RNA, C/D box 8 [ Homo sapiens (human) ]

Gene ID: 319103, updated on 23-Nov-2021

Summary

Official Symbol
SNORD8provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 8provided by HGNC
Primary source
HGNC:HGNC:20159
See related
Ensembl:ENSG00000200785 MIM:618943
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
RNU6C; mgU6-53
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Genomic context

See SNORD8 in Genome Data Viewer
Location:
14q11.2
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (21397293..21397401, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (21865452..21865560, complement)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107984643 Neighboring gene chromodomain helicase DNA binding protein 8 Neighboring gene small nucleolar RNA, C/D box 9 Neighboring gene ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 2 Neighboring gene eukaryotic translation initiation factor 4E binding protein 1 pseudogene 1

Genomic regions, transcripts, and products

Phenotypes

Copy number response

Description
Copy number response
Haploinsufficency

No evidence available (Last evaluated 2015-03-11)

ClinGen Genome Curation Page
Triplosensitivity

No evidence available (Last evaluated 2015-03-11)

ClinGen Genome Curation Page

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • RNA, U6C small nucleolar

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_002916.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL161747
    Related
    ENST00000363915.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    21397293..21397401 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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