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    LINC01475 long intergenic non-protein coding RNA 1475 [ Homo sapiens (human) ]

    Gene ID: 101927324, updated on 10-Oct-2023

    Summary

    Official Symbol
    LINC01475provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 1475provided by HGNC
    Primary source
    HGNC:HGNC:51113
    See related
    Ensembl:ENSG00000257582 AllianceGenome:HGNC:51113
    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
    Biased expression in spleen (RPKM 1.3), small intestine (RPKM 0.4) and 4 other tissues See more
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    Genomic context

    See LINC01475 in Genome Data Viewer
    Location:
    10q24.2
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (99526350..99531177, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (100408313..100413141, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (101286107..101290934, complement)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3870 Neighboring gene GOT1 divergent transcript Neighboring gene uncharacterized LOC124902570 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:101280549-101281428 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:101281429-101282308 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:101282309-101283188 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:101292029-101292920 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2692 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2693 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:101299909-101300617 Neighboring gene NK2 homeobox 3 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3871 Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:101355523-101356023 Neighboring gene small nucleolar RNA U13

    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

    Phenotypes

    EBI GWAS Catalog

    Description
    A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
    EBI GWAS Catalog
    Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
    EBI GWAS Catalog
    Genome-wide association identifies multiple ulcerative colitis susceptibility loci.
    EBI GWAS Catalog
    Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).
    EBI GWAS Catalog
    Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
    EBI GWAS Catalog
    Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
    EBI GWAS Catalog
    Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.
    EBI GWAS Catalog
    Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
    EBI GWAS Catalog
    Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
    EBI GWAS Catalog

    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_120618.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL353719, DQ372722
      Related
      ENST00000548010.1

    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_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      99526350..99531177 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      100408313..100413141 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)