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EOLA2-DT EOLA2 divergent transcript [ Homo sapiens (human) ]

Gene ID: 100272228, updated on 13-May-2022

Summary

Official Symbol
EOLA2-DTprovided by HGNC
Official Full Name
EOLA2 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:48579
See related
Ensembl:ENSG00000235703 AllianceGenome:HGNC:48579
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
LINC00894
Expression
Ubiquitous expression in prostate (RPKM 4.2), thyroid (RPKM 3.9) and 25 other tissues See more
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Genomic context

See EOLA2-DT in Genome Data Viewer
Location:
Xq28
Exon count:
12
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (149938548..150016787)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (148206174..148284407)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (149106766..149185018)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene MAGEA8 antisense RNA 1 Neighboring gene MAGE family member A8 Neighboring gene endothelium and lymphocyte associated ASCH domain 2 Neighboring gene heat shock transcription factor family, X-linked member 4 Neighboring gene nucleolar protein 11 pseudogene Neighboring gene microRNA 2114

Genomic regions, transcripts, and products

Expression

  • 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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • long intergenic non-protein coding RNA 894

Clone Names

  • FLJ30251, FLJ44451

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_027456.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC244099, BC032484, DA306809
    Related
    ENST00000444489.5

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    149938548..150016787
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    148206174..148284407
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)