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    RNVU1-18 RNA, variant U1 small nuclear 18 [ Homo sapiens (human) ]

    Gene ID: 26863, updated on 17-Jun-2019

    Summary

    Official Symbol
    RNVU1-18provided by HGNC
    Official Full Name
    RNA, variant U1 small nuclear 18provided by HGNC
    Primary source
    HGNC:HGNC:37496
    See related
    Ensembl:ENSG00000206737
    Gene type
    snRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    U1.15; U1P15; RNU1-5; RNU1P1; RNU1P9; U1P101; vU1.18; RNU1-25; RNU1-25P

    Genomic context

    See RNVU1-18 in Genome Data Viewer
    Location:
    1q21.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (143729407..143729570, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (149224058..149224221, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene tRNA-Asn (anticodon GTT) 22-1 Neighboring gene RNA, U1 small nuclear 92, pseudogene Neighboring gene tRNA-Asn (anticodon GTT) 6-1 Neighboring gene NBPF member 6 pseudogene

    Genomic regions, transcripts, and products

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Other Names

    • RNA, U1 small nuclear 25, pseudogene
    • RNA, U1 small nuclear 5
    • RNA, U1 small nuclear pseudogene 1
    • RNA, U1 small nuclear pseudogene 9

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    pre-mRNA 5'-splice site binding IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    mRNA 5'-splice site recognition IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    U1 snRNP IEA
    Inferred from Electronic Annotation
    more info
     

    NCBI Reference Sequences (RefSeq)

    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_004400.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC239800
      Related
      ENST00000384010.1

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

      Range
      143729407..143729570 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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