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MED14OS MED14 opposite strand [ Homo sapiens (human) ]

Gene ID: 100873985, updated on 23-Nov-2021

Summary

Official Symbol
MED14OSprovided by HGNC
Official Full Name
MED14 opposite strandprovided by HGNC
Primary source
HGNC:HGNC:40162
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
MED14-AS1
Expression
Ubiquitous expression in kidney (RPKM 1.6), colon (RPKM 1.4) and 24 other tissues See more
Orthologs
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Genomic context

See MED14OS in Genome Data Viewer
Location:
Xp11.4
Exon count:
2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (40735690..40738698)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (40594942..40597950)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene chromosome X open reading frame 38 Neighboring gene mitochondrial pyruvate carrier 1 like Neighboring gene mediator complex subunit 14 Neighboring gene CLDN7 pseudogene 1 Neighboring gene divergent-paired related homeobox pseudogene 6

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

General gene information

Homology

Other Names

  • MED14 antisense RNA 1
  • MED14 antisense gene protein 1
  • MED14 opposite strand protein

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_169211.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC092474

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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    40735690..40738698
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001289773.1: Suppressed sequence

    Description
    NM_001289773.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
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