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LINC01091 long intergenic non-protein coding RNA 1091 [ Homo sapiens (human) ]

Gene ID: 285419, updated on 5-Sep-2025
Official Symbol
LINC01091provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1091provided by HGNC
Primary source
HGNC:HGNC:27721
See related
Ensembl:ENSG00000249464 AllianceGenome:HGNC:27721
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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See LINC01091 in Genome Data Viewer
Location:
4q28.1
Exon count:
8
Annotation release Status Assembly Chr Location
RS_2025_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (123649991..123930778)
RS_2025_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (126953999..127234781)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (124571146..124851933)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377405 Neighboring gene MPRA-validated peak5100 silencer Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:124468793-124469376 Neighboring gene long intergenic non-protein coding RNA 2435 Neighboring gene NANOG hESC enhancer GRCh37_chr4:124485860-124486361 Neighboring gene NANOG hESC enhancer GRCh37_chr4:124506198-124506715 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21881 Neighboring gene Sharpr-MPRA regulatory region 12612 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr4:124521451-124522096 Neighboring gene uncharacterized LOC124900775 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:124670185-124670770 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:124670771-124671354 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:124671355-124671938 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21882 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_72756 Neighboring gene ribosomal protein L21 pseudogene 50 Neighboring gene Sharpr-MPRA regulatory region 6240 Neighboring gene VISTA enhancer hs1525 Neighboring gene uncharacterized LOC124900776 Neighboring gene uncharacterized LOC105377407 Neighboring gene peptidylprolyl isomerase A pseudogene 76

Go to nucleotide: Graphics FASTA GenBank

  • 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

Related articles in PubMed

  1. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

GeneRIFs: Gene References Into Functions

Review eQTL and phenotype association data in this region using PheGenI

See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

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_027105.3 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC096732, AC108075, AI051428, AW771701, BM311133, BX108574
    Related
    ENST00000508111.6

  2. NR_027106.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093767, BC033378
    Related
    ENST00000515769.1

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    123649991..123930778
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    126953999..127234781
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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