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LINC01722 long intergenic non-protein coding RNA 1722 [ Homo sapiens (human) ]

Gene ID: 101929486, updated on 10-Oct-2023

Summary

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Official Symbol
LINC01722provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1722provided by HGNC
Primary source
HGNC:HGNC:52510
See related
Ensembl:ENSG00000233048 AllianceGenome:HGNC:52510
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
Low expression observed in reference dataset See more
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Genomic context

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See LINC01722 in Genome Data Viewer
Location:
20p12.1
Exon count:
12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (12865204..12952519, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (12908606..12995932, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (12845852..12933167, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904871 Neighboring gene uncharacterized LOC105372532 Neighboring gene NANOG hESC enhancer GRCh37_chr20:12681309-12681810 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr20:12728856-12729533 Neighboring gene H3K27ac hESC enhancer GRCh37_chr20:12730880-12731401 Neighboring gene H3K27ac hESC enhancer GRCh37_chr20:12731402-12731922 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr20:12733099-12734064 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:12734065-12735030 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:12735031-12735995 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:12736872-12737427 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr20:12739725-12740236 Neighboring gene MPRA-validated peak4148 silencer Neighboring gene uncharacterized LOC105372535 Neighboring gene uncharacterized LOC102606466 Neighboring gene Sharpr-MPRA regulatory region 3567 Neighboring gene long intergenic non-protein coding RNA 1723 Neighboring gene ReSE screen-validated silencer GRCh37_chr20:12980521-12980692 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr20:13010129-13011328 Neighboring gene serine palmitoyltransferase long chain base subunit 3 Neighboring gene CENATAC pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17549 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17550 Neighboring gene taspase 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12677 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12678 Neighboring gene ISM1 antisense RNA 1 Neighboring gene isthmin 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • 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

Bibliography

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Related articles in PubMed

  1. Voxelwise genome-wide association study (vGWAS). Stein JL, et al. Neuroimage, 2010 Nov 15. PMID 20171287, Free PMC Article
  2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

EBI GWAS Catalog

Description
Voxelwise genome-wide association study (vGWAS).
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

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_109868.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL078623, AL133331, BC036700
    Related
    ENST00000456265.1

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    12865204..12952519 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    12908606..12995932 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases