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LINC02028 long intergenic non-protein coding RNA 2028 [ Homo sapiens (human) ]

Gene ID: 285389, updated on 13-May-2022

Summary

Official Symbol
LINC02028provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2028provided by HGNC
Primary source
HGNC:HGNC:27718
See related
Ensembl:ENSG00000230102 AllianceGenome:HGNC:27718
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 1.2), liver (RPKM 0.5) and 6 other tissues See more
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Genomic context

See LINC02028 in Genome Data Viewer
Location:
3q29
Exon count:
9
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (194005456..194070970, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (196702110..196767637, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (193723245..193788759, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2026 Neighboring gene Sharpr-MPRA regulatory region 6900 Neighboring gene developmental pluripotency associated 2 pseudogene 3 Neighboring gene uncharacterized LOC102724877 Neighboring gene Sharpr-MPRA regulatory region 14852 Neighboring gene hes family bHLH transcription factor 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_136179.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AI701578, BX096813
    Related
    ENST00000458224.5
  2. NR_136180.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC024559, AI701578, AI818666
  3. NR_136181.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC024559
    Related
    ENST00000432154.5

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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    194005456..194070970 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    196702110..196767637 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)