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LINC02301 long intergenic non-protein coding RNA 2301 [ Homo sapiens (human) ]

Gene ID: 101928599, updated on 23-Nov-2021

Summary

Official Symbol
LINC02301provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2301provided by HGNC
Primary source
HGNC:HGNC:53220
See related
Ensembl:ENSG00000258743
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 LINC02301 in Genome Data Viewer
Location:
14q31.1
Exon count:
6
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (82642632..82706825)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (83108976..83173169)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene eukaryotic translation initiation factor 3 subunit L pseudogene 1 Neighboring gene uncharacterized LOC105370599 Neighboring gene endosulfine alpha pseudogene 2 Neighboring gene uncharacterized LOC105370600 Neighboring gene RNA, U7 small nuclear 51 pseudogene

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
A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.
EBI GWAS Catalog

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_146650.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL163171, AL390076
    Related
    ENST00000555150.5

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_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    82642632..82706825
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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