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LINC01682 long intergenic non-protein coding RNA 1682 [ Homo sapiens (human) ]

Gene ID: 101927504, updated on 10-Oct-2023

Summary

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Official Symbol
LINC01682provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1682provided by HGNC
Primary source
HGNC:HGNC:52470
See related
Ensembl:ENSG00000227043 AllianceGenome:HGNC:52470
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 testis (RPKM 1.2) See more
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Genomic context

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Location:
1q42.13
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (229875550..229893908, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (229254823..229273182, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (230011297..230029655, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985464 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:229950786-229951341 Neighboring gene uncharacterized LOC105373162 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:229993502-229993697 Neighboring gene uncharacterized LOC105373163 Neighboring gene MPRA-validated peak757 silencer Neighboring gene long intergenic non-protein coding RNA 1736

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_146473.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL354826

  2. NR_146474.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL354826

  3. NR_146475.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL354826

  4. NR_146476.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL354826
    Related
    ENST00000435973.2

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    229875550..229893908 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    229254823..229273182 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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