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LINC00456 long intergenic non-protein coding RNA 456 [ Homo sapiens (human) ]

Gene ID: 103625683, updated on 10-Oct-2023

Summary

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Official Symbol
LINC00456provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 456provided by HGNC
Primary source
HGNC:HGNC:42804
See related
Ensembl:ENSG00000233124 AllianceGenome:HGNC:42804
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
Restricted expression toward placenta (RPKM 1.1) See more
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Genomic context

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See LINC00456 in Genome Data Viewer
Location:
13q32.1
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (97172382..97179622, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (96376416..96383656, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (97824636..97831876, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124903196 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5449 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:97784629-97785153 Neighboring gene uncharacterized LOC124903197 Neighboring gene muscleblind like splicing regulator 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7887 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:97879323-97880105 Neighboring gene uncharacterized LOC107984573 Neighboring gene uncharacterized LOC101927385 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7888 Neighboring gene Sharpr-MPRA regulatory region 6469

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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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

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_125725.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL359925
    Related
    ENST00000453862.1

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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    97172382..97179622 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    96376416..96383656 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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