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    LINC01436 long intergenic non-protein coding RNA 1436 [ Homo sapiens (human) ]

    Gene ID: 100996609, updated on 10-Dec-2024

    Summary

    Official Symbol
    LINC01436provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 1436provided by HGNC
    Primary source
    HGNC:HGNC:50754
    See related
    Ensembl:ENSG00000231106 AllianceGenome:HGNC:50754
    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
    Broad expression in gall bladder (RPKM 1.3), appendix (RPKM 1.1) and 17 other tissues See more
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    Genomic context

    See LINC01436 in Genome Data Viewer
    Location:
    21q22.12
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (36005320..36008295)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (34388378..34391353)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (37377618..37380593)

    Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene MT-ND2 pseudogene 1 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr21:37324968-37326167 Neighboring gene uncharacterized LOC101928269 Neighboring gene ribosomal protein L23a pseudogene 3 Neighboring gene SET domain containing 4 Neighboring gene ribosomal modification protein rimK like family member B pseudogene 1

    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

    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_110419.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AP000688
      Related
      ENST00000457157.4

    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_000021.9 Reference GRCh38.p14 Primary Assembly

      Range
      36005320..36008295
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060945.1 Alternate T2T-CHM13v2.0

      Range
      34388378..34391353
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)