Format

Send to:

Choose Destination

LINC01559 long intergenic non-protein coding RNA 1559 [ Homo sapiens (human) ]

Gene ID: 283422, updated on 23-Nov-2021

Summary

Official Symbol
LINC01559provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1559provided by HGNC
Primary source
HGNC:HGNC:26598
See related
Ensembl:ENSG00000180861
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
C12orf36
Expression
Biased expression in colon (RPKM 13.2), gall bladder (RPKM 8.1) and 3 other tissues See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See LINC01559 in Genome Data Viewer
Location:
12p13.1
Exon count:
3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (13370671..13376745, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (13523605..13529679, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene epithelial membrane protein 1 Neighboring gene Sharpr-MPRA regulatory region 3500 Neighboring gene RNA, 5S ribosomal pseudogene 353 Neighboring gene RNA, U6 small nuclear 590, pseudogene

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

General gene information

Markers

Clone Names

  • FLJ33810, FLJ97127, MGC120140

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_036555.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC022276, AK091129, BG421494
    Related
    ENST00000318426.6

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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    13370671..13376745 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_182558.1: Suppressed sequence

    Description
    NM_182558.1: This RefSeq was permanently suppressed because it is now thought that this gene does not encode a protein.
Support Center