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

Gene ID: 100507564, updated on 13-May-2022

Summary

Official Symbol
MAGOH-DTprovided by HGNC
Official Full Name
MAGOH divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:49539
See related
Ensembl:ENSG00000226754 AllianceGenome:HGNC:49539
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
Biased expression in testis (RPKM 16.3), thyroid (RPKM 8.5) and 13 other tissues See more
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Genomic context

See MAGOH-DT in Genome Data Viewer
Location:
1p32.3
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (53238610..53242783)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (53120073..53124246)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (53704282..53708455)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene carnitine palmitoyltransferase 2 Neighboring gene CXXC motif containing zinc binding protein Neighboring gene mago homolog, exon junction complex subunit Neighboring gene uncharacterized LOC105378728 Neighboring gene LDL receptor related protein 8 Neighboring gene uncharacterized LOC105378726

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_038953.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC033363
    Related
    ENST00000458151.2

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    53238610..53242783
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    53120073..53124246
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)