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

Gene ID: 100505894, updated on 19-Jul-2022

Summary

Official Symbol
TMEM161B-DTprovided by HGNC
Official Full Name
TMEM161B divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:43839
See related
Ensembl:ENSG00000247828 AllianceGenome:HGNC:43839
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
110 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (88268882..88436674)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (88749932..88917732)
105.20220307 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 transmembrane protein 161B Neighboring gene RNA, 5S ribosomal pseudogene 187 Neighboring gene small nucleolar RNA SNORA70 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

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
    ENST00000657972.3
  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
    ENST00000504922.7
  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 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_000005.10 Reference GRCh38.p14 Primary Assembly

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

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    88749932..88917732
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)