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VSTM2B-DT VSTM2B divergent transcript [ Homo sapiens (human) ]

Gene ID: 284395, updated on 13-May-2022

Summary

Official Symbol
VSTM2B-DTprovided by HGNC
Official Full Name
VSTM2B divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:27615
See related
Ensembl:ENSG00000264515 AllianceGenome:HGNC:27615
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 VSTM2B-DT in Genome Data Viewer
Location:
19q12
Exon count:
10
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (29287009..29525750, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (31818098..32051348, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (29777916..30016657, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene UQCRFS1 divergent transcript Neighboring gene RNA, 7SL, cytoplasmic 340, pseudogene Neighboring gene Sharpr-MPRA regulatory region 9443 Neighboring gene uncharacterized LOC124904683 Neighboring gene V-set and transmembrane domain containing 2B Neighboring gene uncharacterized LOC105372353 Neighboring gene POP4 homolog, ribonuclease P/MRP subunit

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

Phenotypes

EBI GWAS Catalog

Description
Genetic variants associated with disordered eating.
EBI GWAS Catalog
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
EBI GWAS Catalog

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_040029.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC006134, AC007786, AC011474
    Related
    ENST00000582581.5

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_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    29287009..29525750 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    31818098..32051348 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)