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LINC01366 long intergenic non-protein coding RNA 1366 [ Homo sapiens (human) ]

Gene ID: 257358, updated on 13-May-2022

Summary

Official Symbol
LINC01366provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1366provided by HGNC
Primary source
HGNC:HGNC:27416
See related
Ensembl:ENSG00000235172 AllianceGenome:HGNC:27416
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

See LINC01366 in Genome Data Viewer
Location:
5q35.1
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (170331393..170335100)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (170870237..170873944)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (169758397..169762104)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene chromosome 5 open reading frame 58 Neighboring gene lymphocyte cytosolic protein 2 Neighboring gene uncharacterized LOC100128059 Neighboring gene potassium voltage-gated channel interacting protein 1 Neighboring gene KCNIP1 overlapping transcript 1 Neighboring gene potassium calcium-activated channel subfamily M regulatory beta subunit 1

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

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_026945.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longest transcript.
    Source sequence(s)
    AC034199, BQ053612, DB107949, DB343102
  2. NR_108024.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate splice site in the 5' terminal exon, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AK093725, CD518314, DB107949
    Related
    ENST00000662612.1
  3. NR_108025.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) lacks an alternate internal exon, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AK093725, BG494977, DB107949
    Related
    ENST00000665008.1

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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    170331393..170335100
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    170870237..170873944
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001025454.1: Suppressed sequence

    Description
    NM_001025454.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.