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NORAD non-coding RNA activated by DNA damage [ Homo sapiens (human) ]

Gene ID: 647979, updated on 24-Nov-2020

Summary

Official Symbol
NORADprovided by HGNC
Official Full Name
non-coding RNA activated by DNA damageprovided by HGNC
Primary source
HGNC:HGNC:44311
See related
Ensembl:ENSG00000260032 MIM:617037
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
LINC00657

Genomic context

See NORAD in Genome Data Viewer
Location:
20q11.23
Exon count:
1
Annotation release Status Assembly Chr Location
109.20201120 current GRCh38.p13 (GCF_000001405.39) 20 NC_000020.11 (36045618..36050960, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (34633540..34638882, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene PHD finger protein 20 Neighboring gene RNA, U6 small nuclear 937, pseudogene Neighboring gene SCAN domain containing 1 Neighboring gene cyclic nucleotide binding domain containing 2 Neighboring gene erythrocyte membrane protein band 4.1 like 1 Neighboring gene high mobility group box 3 pseudogene 2 Neighboring gene uncharacterized LOC100130373

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Interactions

Products Interactant Other Gene Complex Source Pubs Description

NCBI Reference Sequences (RefSeq)

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_027451.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AI619767, AK090641, AL035420, BC011592
    Related
    ENST00000565493.2

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20201120

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p13 Primary Assembly

    Range
    36045618..36050960 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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