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OBSCN-AS1 OBSCN antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 574407, updated on 25-Jan-2022

Summary

Official Symbol
OBSCN-AS1provided by HGNC
Official Full Name
OBSCN antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:32047
See related
Ensembl:ENSG00000162913 AllianceGenome:HGNC:32047
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
C1orf145
Expression
Low expression observed in reference dataset See more
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Genomic context

See OBSCN-AS1 in Genome Data Viewer
Location:
1q42.13
Exon count:
5
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (228203506..228213664, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (228391207..228401365, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene IBA57 divergent transcript Neighboring gene Sharpr-MPRA regulatory region 12629 Neighboring gene iron-sulfur cluster assembly factor IBA57 Neighboring gene obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF Neighboring gene Sharpr-MPRA regulatory region 4086 Neighboring gene uncharacterized LOC101927401

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

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_073154.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AK056556, AL359510
    Related
    ENST00000337335.5
  2. NR_073155.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks exons and represents an alternate terminal exon, compared to variant 1.
    Source sequence(s)
    AL359510, BC027909
    Related
    ENST00000295012.5

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_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    228203506..228213664 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001025495.2: Suppressed sequence

    Description
    NM_001025495.2: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
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