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GHRLOS ghrelin opposite strand/antisense RNA [ Homo sapiens (human) ]

Gene ID: 100126793, updated on 25-Jan-2022

Summary

Official Symbol
GHRLOSprovided by HGNC
Official Full Name
ghrelin opposite strand/antisense RNAprovided by HGNC
Primary source
HGNC:HGNC:33885
See related
Ensembl:ENSG00000240288 MIM:618445; AllianceGenome:HGNC:33885
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
GHRLAS; GHRL-AS1; NCRNA00068
Summary
This gene is an antisense gene of the ghrelin/obestatin prepropeptide gene. Alternatively spliced transcript variants have been identified and they may function as non-coding regulatory RNAs. [provided by RefSeq, Jan 2013]
Expression
Ubiquitous expression in stomach (RPKM 13.1), bone marrow (RPKM 11.6) and 24 other tissues See more
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Genomic context

See GHRLOS in Genome Data Viewer
Location:
3p25.3
Exon count:
7
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (10280952..10293449)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (10322636..10335133)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene 3p25 TatD DNase domain containing 2 Alu-mediated recombination region Neighboring gene TatD DNase domain containing 2 Neighboring gene Sharpr-MPRA regulatory region 7129 Neighboring gene Sharpr-MPRA regulatory region 4342 Neighboring gene long intergenic non-protein coding RNA 852 Neighboring gene microRNA 12127 Neighboring gene ghrelin and obestatin prepropeptide Neighboring gene SEC13 homolog, nuclear pore and COPII coat complex component Neighboring gene ATPase plasma membrane Ca2+ transporting 2 Neighboring gene microRNA 378b

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Potential readthrough

Included gene: TATDN2

Other Names

  • GHRL antisense RNA 1 (non-protein coding)

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.

Genomic

  1. NG_033090.2 RefSeqGene

    Range
    5001..17498
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. NR_004431.3 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) is represented as non-coding because it lacks a supported ORF.
    Source sequence(s)
    BM991802, EU789528, EU789531, EU789538
    Related
    ENST00000439539.3
  2. NR_024144.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) contains an alternate exon and uses an alternate splice site, compared to variant 1.
    Source sequence(s)
    BM991802, EU789528, EU789531, EU789545
  3. NR_024145.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) contains two alternate exons and lacks an alternate exon, compared to variant 1.
    Source sequence(s)
    BM991802, EU789528, EU789531, EU789537
  4. NR_073566.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (5) contains two alternate exons and uses an alternate splice site, compared to variant 1.
    Source sequence(s)
    BM991802, EU789528, EU789531, EU789543
  5. NR_073567.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (6) contains an alternate exon and uses two alternate splice sites, compared to variant 1.
    Source sequence(s)
    BM991802, EU789528, EU789531, EU789544
  6. NR_073568.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (7) contains an alternate exon and uses an alternate splice site, compared to variant 1.
    Source sequence(s)
    BM991802, EU789528, EU789531, EU789535

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_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    10280952..10293449
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_024146.1: Suppressed sequence

    Description
    NR_024146.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript.
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