Format

Send to:

Choose Destination

LINC01711 long intergenic non-protein coding RNA 1711 [ Homo sapiens (human) ]

Gene ID: 79160, updated on 25-Jan-2022

Summary

Official Symbol
LINC01711provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1711provided by HGNC
Primary source
HGNC:HGNC:28663
See related
Ensembl:ENSG00000268941 AllianceGenome:HGNC:28663
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See LINC01711 in Genome Data Viewer
Location:
20q13.32
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 20 NC_000020.11 (58634772..58635738)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (57209828..57210794)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene APC down-regulated 1 like Neighboring gene APCDD1L divergent transcript Neighboring gene Sharpr-MPRA regulatory region 4326 Neighboring gene uncharacterized LOC107985410 Neighboring gene STX16-NPEPL1 readthrough (NMD candidate) Neighboring gene syntaxin 16

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_125359.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL050327, BC002831, BU624279
    Related
    ENST00000598340.2

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_000020.11 Reference GRCh38.p13 Primary Assembly

    Range
    58634772..58635738
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_024314.2: Suppressed sequence

    Description
    NM_024314.2: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
Support Center