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LINC00355 long intergenic non-protein coding RNA 355 [ Homo sapiens (human) ]

Gene ID: 144766, updated on 19-May-2026
Official Symbol
LINC00355provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 355provided by HGNC
Primary source
HGNC:HGNC:27061
See related
Ensembl:ENSG00000227674 AllianceGenome:HGNC:27061
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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See LINC00355 in Genome Data Viewer
Location:
13q21.31
Exon count:
6
Annotation release Status Assembly Chr Location
RS_2025_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (63986371..64076011, complement)
RS_2025_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (63208203..63297811, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (64560504..64650144, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377815 Neighboring gene NANOG hESC enhancer GRCh37_chr13:64427887-64428388 Neighboring gene nuclear transcription factor Y subunit alpha pseudogene 1 Neighboring gene Sharpr-MPRA regulatory region 7190 Neighboring gene uncharacterized LOC124903237 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:64913635-64914282 Neighboring gene uncharacterized LOC105370238

  • 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

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Markers

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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_145420.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL354736, AL355879
    Related
    ENST00000456627.1

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2025_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    63986371..64076011 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    63208203..63297811 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)