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LINC00861 long intergenic non-protein coding RNA 861 [ Homo sapiens (human) ]

Gene ID: 100130231, updated on 13-May-2022

Summary

Official Symbol
LINC00861provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 861provided by HGNC
Primary source
HGNC:HGNC:45133
See related
Ensembl:ENSG00000245164 AllianceGenome:HGNC:45133
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 lymph node (RPKM 13.9), appendix (RPKM 8.4) and 5 other tissues See more
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Genomic context

See LINC00861 in Genome Data Viewer
Location:
8q24.13
Exon count:
4
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (125922523..125951197, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (127049993..127078671, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (126934767..126963441, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902017 Neighboring gene RNA, U6 small nuclear 442, pseudogene Neighboring gene superoxide dismutase [Cu-Zn]-like Neighboring gene Sharpr-MPRA regulatory region 6550

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

Phenotypes

EBI GWAS Catalog

Description
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.
EBI GWAS Catalog

General gene information

Markers

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_038446.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AC024681
    Related
    ENST00000500989.3
  2. NR_038447.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) represents an alternate 3' splice pattern, compared to variant 1.
    Source sequence(s)
    DA818756, DA944021

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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    125922523..125951197 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    127049993..127078671 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)