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SCARNA8 small Cajal body-specific RNA 8 [ Homo sapiens (human) ]

Gene ID: 677776, updated on 13-May-2022

Summary

Official Symbol
SCARNA8provided by HGNC
Official Full Name
small Cajal body-specific RNA 8provided by HGNC
Primary source
HGNC:HGNC:32564
See related
Ensembl:ENSG00000251733 MIM:615646; AllianceGenome:HGNC:32564
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
U92
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Genomic context

See SCARNA8 in Genome Data Viewer
Location:
9p22.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (19063656..19063786, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (19076523..19076653, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (19063654..19063784, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene stabilizer of axonemal microtubules 1 Neighboring gene proteasome 26S subunit, ATPase 3 pseudogene 1 Neighboring gene Ras related GTP binding A Neighboring gene HAUS augmin like complex subunit 6 Neighboring gene RNA, U6 small nuclear 264, pseudogene Neighboring gene Sharpr-MPRA regulatory region 12241 Neighboring gene perilipin 2

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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 Cajal body IEA
Inferred from Electronic Annotation
more info
 
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_003009.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AY077742
    Related
    ENST00000515924.1

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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    19063656..19063786 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    19076523..19076653 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)