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    ARHGAP5-AS1 ARHGAP5 antisense RNA 1 (head to head) [ Homo sapiens (human) ]

    Gene ID: 84837, updated on 10-Oct-2023

    Summary

    Official Symbol
    ARHGAP5-AS1provided by HGNC
    Official Full Name
    ARHGAP5 antisense RNA 1 (head to head)provided by HGNC
    Primary source
    HGNC:HGNC:20279
    See related
    AllianceGenome:HGNC:20279
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    C14orf128
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    Genomic context

    See ARHGAP5-AS1 in Genome Data Viewer
    Location:
    14q12
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (32075419..32076699, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (26273042..26274322, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (32544625..32545905, complement)

    Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene ZFAND2A pseudogene 2 Neighboring gene MPRA-validated peak2133 silencer Neighboring gene MED14-independent group 3 enhancer GRCh37_chr14:32489479-32490678 Neighboring gene uncharacterized LOC105370440 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5657 Neighboring gene Sharpr-MPRA regulatory region 9862 Neighboring gene Rho GTPase activating protein 5 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr14:32596327-32597277 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8238 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8239 Neighboring gene RNA, U6 small nuclear 7

    Genomic regions, transcripts, and products

    Bibliography

    General gene information

    Markers

    Other Names

    • ARHGAP5 antisense RNA 1 (non-protein coding)

    Clone Names

    • MGC15504

    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_027263.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AI493138, BC007251, BM745256

    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_000014.9 Reference GRCh38.p14 Primary Assembly

      Range
      32075419..32076699 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060938.1 Alternate T2T-CHM13v2.0

      Range
      26273042..26274322 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_032751.1: Suppressed sequence

      Description
      NM_032751.1: This RefSeq was suppressed temporarily based on the calculation that the annotated protein was shorter than a protein or proteins from a putative ortholog.