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CELF2-AS1 CELF2 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 414196, updated on 24-Jul-2021


Official Symbol
CELF2-AS1provided by HGNC
Official Full Name
CELF2 antisense RNA 1provided by HGNC
Primary source
Gene type
RefSeq status
Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
Biased expression in bone marrow (RPKM 6.2), testis (RPKM 1.7) and 6 other tissues See more
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Genomic context

See CELF2-AS1 in Genome Data Viewer
Exon count:
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (11316833..11344674, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (11358796..11386673, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene CUGBP Elav-like family member 2 Neighboring gene CELF2 antisense RNA 2 Neighboring gene Sharpr-MPRA regulatory region 4729 Neighboring gene uncharacterized LOC105376409 Neighboring gene uncharacterized LOC105376411 Neighboring gene USP6 N-terminal like

Genomic regions, transcripts, and products


  • 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

Other Names

  • CELF2 antisense RNA 1 (non-protein coding)

Clone Names

  • FLJ40494

Gene Ontology Provided by GOA

Component Evidence Code Pubs
located_in extracellular region IEA
Inferred from Electronic Annotation
more info

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.


  1. NR_126062.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly


  1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

    11316833..11344674 complement
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001012713.1: Suppressed sequence

    NM_001012713.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
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