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    LASTR lncRNA associated with SART3 regulation of splicing [ Homo sapiens (human) ]

    Gene ID: 105376382, updated on 10-Dec-2024

    Summary

    Official Symbol
    LASTRprovided by HGNC
    Official Full Name
    lncRNA associated with SART3 regulation of splicingprovided by HGNC
    Primary source
    HGNC:HGNC:54143
    See related
    Ensembl:ENSG00000242147 MIM:618938; AllianceGenome:HGNC:54143
    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
    LINC02657
    Expression
    Low expression observed in reference dataset See more
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    Genomic context

    See LASTR in Genome Data Viewer
    Location:
    10p15.1
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (5594984..5596118, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (5598813..5599947, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (5636947..5638081, complement)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376380 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:5595464-5595987 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:5595988-5596510 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:5599714-5600036 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:5602693-5603194 Neighboring gene uncharacterized LOC105376381 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:5605907-5606133 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_13268 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:5616073-5616688 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:5625367-5625895 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:5626502-5627701 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:5629384-5630191 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_13345 Neighboring gene Sharpr-MPRA regulatory region 6566 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:5638569-5639441 Neighboring gene long intergenic non-protein coding RNA 2678 Neighboring gene long intergenic non-protein coding RNA 2677

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    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_134491.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      BF218358, BG035368, CF130727
      Related
      ENST00000478294.3

    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_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      5594984..5596118 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      5598813..5599947 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)