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    LINC00632 long intergenic non-protein coding RNA 632 [ Homo sapiens (human) ]

    Gene ID: 286411, updated on 10-Dec-2024

    Summary

    Official Symbol
    LINC00632provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 632provided by HGNC
    Primary source
    HGNC:HGNC:27865
    See related
    Ensembl:ENSG00000203930 AllianceGenome:HGNC:27865
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ARST; BMOR; ASINC; MDHDH; CDR1as; ciRS-7; CDR1-AS; CDR1NAT
    Expression
    Biased expression in brain (RPKM 3.1), fat (RPKM 0.6) and 2 other tissues See more
    NEW
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    Try the new Transcript table

    Genomic context

    See LINC00632 in Genome Data Viewer
    Location:
    Xq27.1
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (140709759..140791357)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (139021766..139108724)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (139791924..139873522)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105373344 Neighboring gene NANOG hESC enhancer GRCh37_chrX:139608152-139608653 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:139655621-139655814 Neighboring gene uncharacterized LOC101928833 Neighboring gene NANOG hESC enhancer GRCh37_chrX:139805503-139806004 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:139865334-139866831 Neighboring gene microRNA 320d-2 Neighboring gene SPANX family member B1

    Genomic regions, transcripts, and products

    Expression

    • 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

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Other Names

    • ALDOA related specific transcript
    • CDR1 antisense RNA
    • alternatively spliced into CiRS-7
    • brain metastasis oncogenic lncRNA
    • malate dehydrogenase degradation helper

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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_028344.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longest transcript.
      Source sequence(s)
      AK054978, BQ343502, DA082671, DB307877
      Related
      ENST00000370535.8
    2. NR_028345.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an exon and its 3' terminal exon extends past a splice site used in variant 1, resulting in a shorter transcript, compared to variant 1.
      Source sequence(s)
      DA128399, DA529197
    3. NR_104228.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) lacks an exon and contains two alternate 3' exons, resulting in a shorter transcript, compared to variant 1.
      Source sequence(s)
      AL078639, BM811380, DA082671
      Related
      ENST00000498732.9
    4. NR_173139.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL078639, AL844175
      Related
      ENST00000650128.1
    5. NR_173140.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL078639, AL844175
      Related
      ENST00000649329.1
    6. NR_173141.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL078639
      Related
      ENST00000625883.2
    7. NR_173142.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL078639
    8. NR_173143.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL078639
      Related
      ENST00000650391.2
    9. NR_173144.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL078639, AL844175
      Related
      ENST00000648186.1
    10. NR_190227.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL078639

    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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      140709759..140791357
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      139021766..139108724
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)