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LINC01632 long intergenic non-protein coding RNA 1632 [ Homo sapiens (human) ]

Gene ID: 101929826, updated on 17-Sep-2024

Summary

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Official Symbol
LINC01632provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1632provided by HGNC
Primary source
HGNC:HGNC:52419
See related
AllianceGenome:HGNC:52419
Gene type
ncRNA
RefSeq status
MODEL
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 LINC01632 in Genome Data Viewer
Location:
1q21.1
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (144623919..144632587, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (143433906..143443134)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985110 Neighboring gene peptidylprolyl isomerase A like 4F Neighboring gene Sharpr-MPRA regulatory region 1883 duplicate 3 Neighboring gene uncharacterized LOC105371215 Neighboring gene lysine methyltransferase 2C pseudogene 1 Neighboring gene NANOG hESC enhancer GRCh37_chr1:148884967-148885468 Neighboring gene dopamine receptor D5 pseudogene 2

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 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 studies and variants in dbVar

See Variation Viewer (GRCh38)

Genotypes

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    144623919..144632587 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_001737747.2 RNA Sequence

  2. XR_001737748.2 RNA Sequence

  3. XR_007066570.1 RNA Sequence

  4. XR_426815.4 RNA Sequence

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NT_187520.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    134769..143997 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_430635.5 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    143433906..143443134
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007070626.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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