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

Gene ID: 255512, updated on 23-Nov-2021

Summary

Official Symbol
TOLLIP-DTprovided by HGNC
Official Full Name
TOLLIP divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:27403
See related
Ensembl:ENSG00000255153
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
TOLLIP-AS1
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Genomic context

See TOLLIP-DT in Genome Data Viewer
Location:
11p15.5
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (1309708..1310707)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (1330938..1331937)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene mucin 5B, oligomeric mucus/gel-forming Neighboring gene microRNA 6744 Neighboring gene toll interacting protein Neighboring gene uncharacterized LOC105376512 Neighboring gene long intergenic non-protein coding RNA 2689 Neighboring gene BR serine/threonine kinase 2 Neighboring gene uncharacterized LOC107984298

Genomic regions, transcripts, and products

General gene information

Other Names

  • CTD-2245O6.1
  • TOLLIP antisense RNA 1 (head to head)

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_029409.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC034741, DA359936
    Related
    ENST00000530897.1

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_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    1309708..1310707
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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