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LINC00898 long intergenic non-protein coding RNA 898 [ Homo sapiens (human) ]

Gene ID: 400932, updated on 13-May-2022

Summary

Official Symbol
LINC00898provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 898provided by HGNC
Primary source
HGNC:HGNC:48581
See related
Ensembl:ENSG00000205634 AllianceGenome:HGNC:48581
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
Restricted expression toward testis (RPKM 1.2) See more
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Genomic context

See LINC00898 in Genome Data Viewer
Location:
22q13.31
Exon count:
6
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (47621043..47631569, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (48112282..48122803, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (48016792..48027318, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 13395 Neighboring gene long intergenic non-protein coding RNA 1644 Neighboring gene Sharpr-MPRA regulatory region 4711 Neighboring gene epigenetically induced MYC interacting lncRNA 1 Neighboring gene uncharacterized LOC124905150

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

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_033377.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL117329, Z83854
    Related
    ENST00000380990.5

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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    47621043..47631569 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    48112282..48122803 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001001693.1: Suppressed sequence

    Description
    NM_001001693.1: This RefSeq was permanently suppressed because currently sufficient data to support the encoded protein do not exist and the transcript is a nonsense-mediated mRNA decay (NMD) candidate.