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LINC02755 long intergenic non-protein coding RNA 2755 [ Homo sapiens (human) ]

Gene ID: 105376605, updated on 10-Oct-2023

Summary

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Official Symbol
LINC02755provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2755provided by HGNC
Primary source
HGNC:HGNC:54275
See related
Ensembl:ENSG00000254530 AllianceGenome:HGNC:54275
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

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Location:
11p14.1
Exon count:
7
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (29335878..29594350, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (29470799..29729242, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2742 Neighboring gene olfactory receptor family 2 subfamily BH member 1 pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:29072733-29073233 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4551 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4552 Neighboring gene eukaryotic translation elongation factor 1 alpha 1 pseudogene 47 Neighboring gene microtubule affinity regulating kinase 2 pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4553 Neighboring gene long intergenic non-protein coding RNA 2546 Neighboring gene heterogeneous nuclear ribonucleoprotein R pseudogene 2

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • 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

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

Genotypes

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_183753.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC090124, AC110058, AL138813
    Related
    ENST00000653616.1

  2. NR_183754.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC090124, AC110058
    Related
    ENST00000525097.1

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    29335878..29594350 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    29470799..29729242 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases