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LINC02493 long intergenic non-protein coding RNA 2493 [ Homo sapiens (human) ]

Gene ID: 101929123, updated on 17-Sep-2024

Summary

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Official Symbol
LINC02493provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2493provided by HGNC
Primary source
HGNC:HGNC:53477
See related
Ensembl:ENSG00000250819 AllianceGenome:HGNC:53477
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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See LINC02493 in Genome Data Viewer
Location:
4p15.32
Exon count:
6
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (17171757..17186057, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (17153714..17168047, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (17173380..17187680, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105374507 Neighboring gene MT-ND5 pseudogene 4 Neighboring gene ReSE screen-validated silencer GRCh37_chr4:17089199-17089385 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21348 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:17164733-17165234 Neighboring gene uncharacterized LOC107986219 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:17286136-17286636 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:17286637-17287137 Neighboring gene small nucleolar RNA, H/ACA box 75B

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 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

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

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_125919.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC006231
    Related
    ENST00000509964.1

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    17171757..17186057 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    17153714..17168047 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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