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CELF2-AS2 CELF2 antisense RNA 2 [ Homo sapiens (human) ]

Gene ID: 439950, updated on 13-May-2022

Summary

Official Symbol
CELF2-AS2provided by HGNC
Official Full Name
CELF2 antisense RNA 2provided by HGNC
Primary source
HGNC:HGNC:44703
See related
Ensembl:ENSG00000237986 AllianceGenome:HGNC:44703
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Restricted expression toward testis (RPKM 1.4) See more
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Genomic context

See CELF2-AS2 in Genome Data Viewer
Location:
10p14
Exon count:
7
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (11071541..11105488, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (11081816..11115775, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (11113504..11147451, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene CUGBP Elav-like family member 2 Neighboring gene long intergenic non-protein coding RNA 710 Neighboring gene uncharacterized LOC124902376 Neighboring gene Sharpr-MPRA regulatory region 4729 Neighboring gene Sharpr-MPRA regulatory region 12202

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_046108.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC046381, DB336852
    Related
    ENST00000661890.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    11071541..11105488 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    11081816..11115775 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)