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LINC01213 long intergenic non-protein coding RNA 1213 [ Homo sapiens (human) ]

Gene ID: 101927992, updated on 10-Dec-2024

Summary

Official Symbol
LINC01213provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1213provided by HGNC
Primary source
HGNC:HGNC:49648
See related
Ensembl:ENSG00000244541 AllianceGenome:HGNC:49648
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 LINC01213 in Genome Data Viewer
Location:
3q25.1
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (150238519..150240206)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (152989722..152991410)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (149956306..149957993)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1998 Neighboring gene uncharacterized LOC105374313 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr3:149824644-149825232 Neighboring gene ribosomal protein L32 pseudogene 9 Neighboring gene Sharpr-MPRA regulatory region 11247 Neighboring gene NANOG hESC enhancer GRCh37_chr3:149920455-149920956 Neighboring gene uncharacterized LOC124906376 Neighboring gene uncharacterized LOC105374154 Neighboring gene long intergenic non-protein coding RNA 1214

Genomic regions, transcripts, and products

Expression

  • Project title: Tissue-specific circular RNA induction during human fetal development
  • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
  • BioProject: PRJNA270632
  • Publication: PMID 26076956
  • Analysis date: Mon Apr 2 22:54:59 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_110167.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AC117386, BF676681
    Related
    ENST00000725884.1
  2. NR_110168.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate 5' most exon which results in a shorter transcript compared to variant 1.
    Source sequence(s)
    AC117386, AW195433

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    150238519..150240206
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    152989722..152991410
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)