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LINC00668 long intergenic non-protein coding RNA 668 [ Homo sapiens (human) ]

Gene ID: 400643, updated on 12-Oct-2019

Summary

Official Symbol
LINC00668provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 668provided by HGNC
Primary source
HGNC:HGNC:44328
See related
Ensembl:ENSG00000265933
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
Biased expression in testis (RPKM 11.7), colon (RPKM 6.5) and 4 other tissues See more

Genomic context

See LINC00668 in Genome Data Viewer
Location:
18p11.31
Exon count:
7
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 18 NC_000018.10 (6925474..6929869, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (6919275..6929868, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985176 Neighboring gene RNA, 7SL, cytoplasmic 282, pseudogene Neighboring gene uncharacterized LOC101927168 Neighboring gene Rho GTPase activating protein 28 Neighboring gene uncharacterized LOC101927188 Neighboring gene RNA, U6 small nuclear 916, pseudogene Neighboring gene SCML2 pseudogene 1 Neighboring gene laminin subunit alpha 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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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_034100.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AP005210
    Related
    ENST00000581571.5

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000018.10 Reference GRCh38.p13 Primary Assembly

    Range
    6925474..6929869 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001103383.1: Suppressed sequence

    Description
    NM_001103383.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
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