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DANT2 DXZ4 associated non-coding transcript 2, distal [ Homo sapiens (human) ]

Gene ID: 642776, updated on 12-Oct-2019

Summary

Official Symbol
DANT2provided by HGNC
Official Full Name
DXZ4 associated non-coding transcript 2, distalprovided by HGNC
Primary source
HGNC:HGNC:50862
See related
Ensembl:ENSG00000235244 MIM:301004
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

Genomic context

See DANT2 in Genome Data Viewer
Location:
Xq23
Exon count:
4
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (115840396..115969111, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene eukaryotic translation elongation factor 1 gamma pseudogene 5 Neighboring gene small ubiquitin-like modifier 2 Neighboring gene DXZ4 associated non-coding transcript 1, proximal Neighboring gene RNA, 7SL, cytoplasmic 712, pseudogene Neighboring gene aldo-keto reductase family 1 member B1 pseudogene 8

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000023.11 Chromosome X Reference GRCh38.p13 Primary Assembly

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

  • DXZ4 associated noncoding transcript 2

NCBI Reference Sequences (RefSeq)

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_130730.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AL772226, BC003645, BX642309
    Related
    ENST00000430756.2
  2. NR_132337.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks two exons and includes one alternate exon, compared to variant 1.
    Source sequence(s)
    BM925596, BX642309, CR753863

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    115840396..115969111 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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