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TMEM161B-DT TMEM161B divergent transcript [ Homo sapiens (human) ]

Gene ID: 100505894, updated on 14-Dec-2021

Summary

Official Symbol
TMEM161B-DTprovided by HGNC
Official Full Name
TMEM161B divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:43839
See related
Ensembl:ENSG00000247828
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
TMEM161B-AS1; linc-POLR3G-8
Expression
Ubiquitous expression in brain (RPKM 2.9), kidney (RPKM 2.1) and 24 other tissues See more
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Genomic context

See TMEM161B-DT in Genome Data Viewer
Location:
5q14.3
Exon count:
9
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 5 NC_000005.10 (88268882..88436674)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (87564699..87732491)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379070 Neighboring gene uncharacterized LOC112267943 Neighboring gene transmembrane protein 161B Neighboring gene RNA, 5S ribosomal pseudogene 187 Neighboring gene RPS3A pseudogene 22 Neighboring gene long intergenic non-protein coding RNA 2060 Neighboring gene CRE1 CAGE-defined tissue-specific enhancer Neighboring gene long intergenic non-protein coding RNA 461 Neighboring gene H3 histone pseudogene 23 Neighboring gene microRNA 9-2

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

  • CTC-358I24.1
  • TMEM161B 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_039993.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This is variant 1.
    Source sequence(s)
    BC030122, BF056341, BM719684
    Related
    ENST00000501869.7
  2. NR_039994.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) contains an alternate 5' terminal exon, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    BF056341, BF672668, HY089208
    Related
    ENST00000657972.2
  3. NR_039995.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) lacks an internal exon, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    BF056341, BM719684, CN260565
    Related
    ENST00000504922.6
  4. NR_105019.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (4) contains an alternate 5' terminal exon and four additional internal exons, resulting in a longer transcript, compared to variant 1.
    Source sequence(s)
    AC016555, BC047059, BF056341, HY089208
    Related
    ENST00000501715.6
  5. NR_105020.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (5) lacks two exons and contains an alternate 5' terminal exon, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    BF056341, DA317999, DA782199

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_000005.10 Reference GRCh38.p13 Primary Assembly

    Range
    88268882..88436674
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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