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    LINC01572 long intergenic non-protein coding RNA 1572 [ Homo sapiens (human) ]

    Gene ID: 101927957, updated on 22-Oct-2024

    Summary

    Official Symbol
    LINC01572provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 1572provided by HGNC
    Primary source
    HGNC:HGNC:51385
    See related
    Ensembl:ENSG00000261008 AllianceGenome:HGNC:51385
    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
    Low expression observed in reference dataset See more
    Orthologs
    NEW
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    Genomic context

    See LINC01572 in Genome Data Viewer
    Location:
    16q22.2
    Exon count:
    16
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (72280902..72664970, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (78097218..78481445, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (72314801..72698869, complement)

    Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene polyamine modulated factor 1 binding protein 1 Neighboring gene uncharacterized LOC105371341 Neighboring gene VISTA enhancer hs22 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr16:72257113-72258312 Neighboring gene uncharacterized LOC124903720 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr16:72319061-72319706 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr16:72324412-72325611 Neighboring gene MYC binding protein pseudogene Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_44023 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_44041 Neighboring gene VISTA enhancer hs108 Neighboring gene uncharacterized LOC124903812 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_44094 Neighboring gene uncharacterized LOC124903718 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_44118 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11096 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_44155 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11097 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:72660846-72661404 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11098 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11099 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11100 Neighboring gene Sharpr-MPRA regulatory region 2952 Neighboring gene ZFHX3 antisense RNA 1 Neighboring gene VISTA enhancer hs20 Neighboring gene RNA, U7 small nuclear 90 pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr16:72756067-72756616 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr16:72756617-72757164 Neighboring gene keratin 18 pseudogene 18

    Genomic regions, transcripts, and products

    Expression

    • 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

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    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_126330.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC009075, AL525401, AL706640, BX327638, BX371395
    2. NR_159370.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC004158, AC010748, AC092289
      Related
      ENST00000662171.1
    3. NR_159371.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC004158, AC010748
    4. NR_159372.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC004158, AC010748, AC092289
      Related
      ENST00000766037.1

    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_000016.10 Reference GRCh38.p14 Primary Assembly

      Range
      72280902..72664970 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060940.1 Alternate T2T-CHM13v2.0

      Range
      78097218..78481445 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)