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

Gene ID: 138948, updated on 13-May-2022

Summary

Official Symbol
DBH-AS1provided by HGNC
Official Full Name
DBH antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:24155
See related
Ensembl:ENSG00000225756 AllianceGenome:HGNC:24155
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
NCRNA00118
Expression
Biased expression in adrenal (RPKM 13.7), liver (RPKM 5.5) and 7 other tissues See more
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Genomic context

See DBH-AS1 in Genome Data Viewer
Location:
9q34.2
Exon count:
2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (133654587..133657408, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (145870600..145873421, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (136519709..136522530, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene ADAMTS like 2 Neighboring gene uncharacterized LOC124902296 Neighboring gene family with sequence similarity 163 member B Neighboring gene dopamine beta-hydroxylase Neighboring gene SARDH intron CAGE-defined T cell enhancer Neighboring gene sarcosine dehydrogenase Neighboring gene Sharpr-MPRA regulatory region 10163

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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

General gene information

Markers

Other Names

  • BPR
  • DBH 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.

RNA

  1. NR_102735.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AF129263, AF129264, AL365494, BQ445882
    Related
    ENST00000425189.1

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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    133654587..133657408 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    145870600..145873421 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_002783.1: Suppressed sequence

    Description
    NR_002783.1: This RefSeq was temporarily suppressed because currently there is not sufficient data to support this transcript.