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TMED2-DT TMED2 divergent transcript [ Homo sapiens (human) ]

Gene ID: 101927415, updated on 25-Jan-2022

Summary

Official Symbol
TMED2-DTprovided by HGNC
Official Full Name
TMED2 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:53346
See related
AllianceGenome:HGNC:53346
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

See TMED2-DT in Genome Data Viewer
Location:
12q24.31
Exon count:
3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (123581066..123584327, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (124065613..124068874, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene Rab interacting lysosomal protein like 1 Neighboring gene Sharpr-MPRA regulatory region 11641 Neighboring gene microRNA 3908 Neighboring gene transmembrane p24 trafficking protein 2 Neighboring gene uncharacterized LOC105370041 Neighboring gene DEAD-box helicase 55 Neighboring gene small nucleolar RNA, H/ACA box 9B

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

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_110049.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC055713, AK125282

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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    123581066..123584327 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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