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LINC01012 long intergenic non-protein coding RNA 1012 [ Homo sapiens (human) ]

Gene ID: 100507173, updated on 13-May-2022

Summary

Official Symbol
LINC01012provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1012provided by HGNC
Primary source
HGNC:HGNC:48986
See related
Ensembl:ENSG00000281706 AllianceGenome:HGNC:48986
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 LINC01012 in Genome Data Viewer
Location:
6p22.1
Exon count:
4
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (27694035..27710222)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (27563696..27579886)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (27661814..27678001)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene tRNA-Thr (anticodon AGT) 2-2 Neighboring gene CRISPRi-validated cis-regulatory element chr6.1284 Neighboring gene tRNA-Ile (anticodon AAT) 2-1 Neighboring gene uncharacterized LOC124901291 Neighboring gene tRNA-Leu (anticodon TAA) 2-1 Neighboring gene tRNA-Thr (anticodon AGT) 4-1

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_038292.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longest transcript.
    Source sequence(s)
    AL009179, BC035101
    Related
    ENST00000629732.1
  2. NR_038293.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate splice site in the 5' region and contains an alternate 3' exon, compared to variant 1.
    Source sequence(s)
    AL009179, AL120625
  3. NR_038294.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) uses an alternate splice site in the 5' region and contains two alternate 3' exons, compared to variant 1.
    Source sequence(s)
    AL120625, BI771077
    Related
    ENST00000628762.2

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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    27694035..27710222
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    27563696..27579886
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)