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

Gene ID: 84837, updated on 23-Nov-2021

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
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
109.20211119 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (32075419..32076699, complement)
105.20201022 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 long intergenic non-protein coding RNA 2313 Neighboring gene uncharacterized LOC105370440 Neighboring gene Rho GTPase activating protein 5 Neighboring gene RNA, U6 small nuclear 7 Neighboring gene RNA, U6 small nuclear 8

Genomic regions, transcripts, and products

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: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    32075419..32076699 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.
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