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LINC02256 long intergenic non-protein coding RNA 2256 [ Homo sapiens (human) ]

Gene ID: 100996255, updated on 23-Nov-2021

Summary

Official Symbol
LINC02256provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2256provided by HGNC
Primary source
HGNC:HGNC:53157
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
Ubiquitous expression in thyroid (RPKM 1.2), ovary (RPKM 1.1) and 25 other tissues See more
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Genomic context

See LINC02256 in Genome Data Viewer
Location:
15q13.3
Exon count:
3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (32536759..32580609)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (32828960..32872810)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene MPHOSPH10 pseudogene 2 Neighboring gene uncharacterized LOC107987222 Neighboring gene WHAMM pseudogene 1 Neighboring gene uncharacterized LOC101928042 Neighboring gene 15q13 distal microdeletion recombination region Neighboring gene golgin A8 family member N Neighboring gene ARHGAP11A-SCG5 readthrough Neighboring gene RNA, 7SL, cytoplasmic 286, pseudogene Neighboring gene Rho GTPase activating protein 11A

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_102756.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC123768, BC037839

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_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    32536759..32580609
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 PATCHES

Genomic

  1. NW_011332701.1 Reference GRCh38.p13 PATCHES

    Range
    4588887..4632737
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 PATCHES

Genomic

  1. NW_012132920.1 Reference GRCh38.p13 PATCHES

    Range
    2055117..2098953
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_2

Genomic

  1. NT_187660.1 Reference GRCh38.p13 ALT_REF_LOCI_2

    Range
    4751339..4795189
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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