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LINC00528 long intergenic non-protein coding RNA 528 [ Homo sapiens (human) ]

Gene ID: 200298, updated on 23-Nov-2021

Summary

Official Symbol
LINC00528provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 528provided by HGNC
Primary source
HGNC:HGNC:26875
See related
Ensembl:ENSG00000269220
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
C22orf37
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Genomic context

See LINC00528 in Genome Data Viewer
Location:
22q11.21
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 22 NC_000022.11 (17777290..17779481)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (18260056..18262247)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene BCL2 like 13 Neighboring gene microRNA 3198-1 Neighboring gene nonconserved acetylation island sequence 74 enhancer Neighboring gene BH3 interacting domain death agonist Neighboring gene VISTA enhancer hs2543 Neighboring gene microtubule associated monooxygenase, calponin and LIM domain containing 3

Genomic regions, transcripts, and products

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_103718.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC016026, AK097861, AW406974, DB114556
    Related
    ENST00000600723.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p13 Primary Assembly

    Range
    17777290..17779481
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_178503.2: Suppressed sequence

    Description
    NM_178503.2: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
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