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LIN28B-AS1 LIN28B antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 100113403, updated on 25-Jan-2022

Summary

Official Symbol
LIN28B-AS1provided by HGNC
Official Full Name
LIN28B antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:21553
See related
Ensembl:ENSG00000203809 AllianceGenome:HGNC:21553
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
C6orf220; LINC00577; dJ439I14.1
Expression
Low expression observed in reference dataset See more
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Genomic context

See LIN28B-AS1 in Genome Data Viewer
Location:
6q16.3
Exon count:
3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (104936294..104940527, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (105384169..105388402, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 Neighboring gene Sharpr-MPRA regulatory region 9880 Neighboring gene poly(A) binding protein cytoplasmic 4 pseudogene Neighboring gene lin-28 homolog B Neighboring gene RNA, U6 small nuclear 1106, pseudogene Neighboring gene blood vessel epicardial substance

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

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_046407.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL135911, AL357315
    Related
    ENST00000369123.3

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_000006.12 Reference GRCh38.p13 Primary Assembly

    Range
    104936294..104940527 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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