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LINC00621 long intergenic non-protein coding RNA 621 [ Homo sapiens (human) ]

Gene ID: 100996930, updated on 10-Oct-2023

Summary

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Official Symbol
LINC00621provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 621provided by HGNC
Primary source
HGNC:HGNC:44227
See related
AllianceGenome:HGNC:44227
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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Location:
13q12.12
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (22876392..22916369, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (22075294..22117275, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (23450531..23490508, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene inositol polyphosphate multikinase pseudogene 1 Neighboring gene Rieske (Fe-S) domain containing pseudogene 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:23433285-23434072 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7448 Neighboring gene uncharacterized LOC105370109 Neighboring gene NANOG hESC enhancer GRCh37_chr13:23460806-23461307 Neighboring gene BASP1 pseudogene 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:23489315-23490228 Neighboring gene collagen alpha-1(III) chain-like Neighboring gene NUS1 pseudogene 2 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_32642 Neighboring gene uncharacterized LOC105370111

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. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560, Free PMC Article
  2. Complete sequencing and characterization of 21,243 full-length human cDNAs. Ota T, et al. Nat Genet, 2004 Jan. PMID 14702039

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

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

General gene information

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Markers

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_138043.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AK091626, AL157931, DA752665

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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    22876392..22916369 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    22075294..22117275 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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