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CHKB-DT CHKB divergent transcript [ Homo sapiens (human) ]

Gene ID: 100144603, updated on 12-Nov-2022

Summary

Official Symbol
CHKB-DTprovided by HGNC
Official Full Name
CHKB divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:40146
See related
Ensembl:ENSG00000205559 AllianceGenome:HGNC:40146
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
HRAT; CHKB-AS1
Expression
Broad expression in testis (RPKM 1.6), prostate (RPKM 1.0) and 24 other tissues See more
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Genomic context

See CHKB-DT in Genome Data Viewer
Location:
22q13.33
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (50583026..50595281)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (51093554..51105799)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (51021455..51033710)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene CHKB-CPT1B readthrough (NMD candidate) Neighboring gene carnitine palmitoyltransferase 1B Neighboring gene Sharpr-MPRA regulatory region 1531 Neighboring gene choline kinase beta Neighboring gene mitogen-activated protein kinase 8 interacting protein 2 Neighboring gene Sharpr-MPRA regulatory region 5053

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

Other Names

  • CHKB antisense RNA 1 (head to head)
  • CTA-384D8.20
  • TCONS_00029632
  • lncRNA-Hypoxia/reoxygenation-associated transcript

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_021492.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks three exons and contains an alternate 3' terminal exon, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    BE393070, BJ989458, CR456603, CR980518
    Related
    ENST00000380711.3
  2. NR_110536.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    BI561134, CR456603

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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    50583026..50595281
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    51093554..51105799
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)