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    LINC01622 long intergenic non-protein coding RNA 1622 [ Homo sapiens (human) ]

    Gene ID: 285768, updated on 10-Dec-2024

    Summary

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    Official Symbol
    LINC01622provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 1622provided by HGNC
    Primary source
    HGNC:HGNC:27768
    See related
    Ensembl:ENSG00000286785 AllianceGenome:HGNC:27768
    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 testis (RPKM 4.0) and kidney (RPKM 1.2) See more
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    Genomic context

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    See LINC01622 in Genome Data Viewer
    Location:
    6p25.3
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (961003..1101332, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (821695..963078, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (961241..1101567, complement)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101927691 Neighboring gene uncharacterized LOC124901236 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:927074-927574 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:927575-928075 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:961366-961866 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:961867-962367 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:995434-995953 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23860 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23859 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23861 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23862 Neighboring gene NANOG hESC enhancer GRCh37_chr6:1028326-1028839 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr6:1066368-1067567 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr6:1100679-1101878 Neighboring gene NANOG hESC enhancer GRCh37_chr6:1104324-1104899 Neighboring gene uncharacterized LOC124901237 Neighboring gene small nucleolar RNA U13

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • 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

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    Related articles in PubMed

    1. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    General gene information

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    Markers

    Other Names

    • TCONS_00011202

    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_027115.3 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longer transcript.
      Source sequence(s)
      BC037855, BC117448
      Related
      ENST00000662378.1

    2. NR_027116.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an internal exon, compared to variant 1.
      Source sequence(s)
      BC037855, BC117448

    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_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      961003..1101332 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      821695..963078 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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