Jpx Jpx transcript, Xist activator (non-protein coding) [Mus musculus (house mouse)] - Gene

Summary

Official Symbol: Jpxprovided by MGI
Official Full Name: Jpx transcript, Xist activator (non-protein coding)provided by MGI
Primary source: MGI:MGI:2180008
See related: Ensembl:ENSMUSG00000097571 AllianceGenome:MGI:2180008
Gene type: ncRNA
RefSeq status: VALIDATED
Organism: Mus musculus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Also known as: Enox; 2010000I03Rik; 2510040I06Rik
Summary: Acts upstream of or within positive regulation of transcription by RNA polymerase II. Orthologous to human JPX (JPX transcript, XIST activator). [provided by Alliance of Genome Resources, Dec 2024]
Expression: Ubiquitous expression in whole brain E14.5 (RPKM 1.4), CNS E14 (RPKM 1.3) and 27 other tissues See more
Orthologs: human all
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Genomic context

Location:: X D; X 46.17 cM

Exon count:: 3

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCm39 (GCF_000001635.27)	X	NC_000086.8 (102537164..102550031)
108.20200622	previous assembly	GRCm38.p6 (GCF_000001635.26)	X	NC_000086.7 (103493558..103506425)

Chromosome X - NC_000086.8 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

lncRNA JPX Promotes Tumor Progression by Interacting with and Destabilizing YTHDF2 in Cutaneous Melanoma.
Title: lncRNA JPX Promotes Tumor Progression by Interacting with and Destabilizing YTHDF2 in Cutaneous Melanoma.
lncRNA JPX-Enriched Chromatin Microenvironment Mediates Vascular Smooth Muscle Cell Senescence and Promotes Atherosclerosis.
Title: lncRNA JPX-Enriched Chromatin Microenvironment Mediates Vascular Smooth Muscle Cell Senescence and Promotes Atherosclerosis.
LncRNA JPX targets SERCA2a to mitigate myocardial ischemia/reperfusion injury by binding to EZH2.
Title: LncRNA JPX targets SERCA2a to mitigate myocardial ischemia/reperfusion injury by binding to EZH2.
Data indicate functional and mechanistic insight for lncRNA activity in mice, and suggest that long noncoding RNA (lncRNA)Jpx is a competence factor for the long noncoding RNA (lncRNA) Xist activation in vivo.
Title: LncRNA Jpx induces Xist expression in mice using both trans and cis mechanisms.
Study demonstrates that molecular titration between an X-encoded RNA and an autosomally encoded protein dictates Xist induction; in pre-XCI cells, CTCF protein represses Xist transcription. At the onset of XCI, Jpx RNA is upregulated, binds CTCF, and extricates CTCF from one Xist allele.
Title: Jpx RNA activates Xist by evicting CTCF.
Jpx is developmentally regulated and accumulates during XCI. Deleting Jpx blocks XCI and is female lethal.
Title: The long noncoding RNA, Jpx, is a molecular switch for X chromosome inactivation.

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Variation

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Alleles

Alleles of this type are documented at Mouse Genome Informatics (MGI)

Endonuclease-mediated (3) 1 citation

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Markers

D10Mit157.2 (e-PCR), detects polymorphism
- UniSTS:126061

PMC196458P2 (e-PCR)
- UniSTS:271806

Gene Ontology Provided by MGI

Function	Evidence Code	Pubs
enables molecular_function	ND No biological Data available more info

Process	Evidence Code	Pubs
acts_upstream_of_or_within positive regulation of transcription by RNA polymerase II	IGI Inferred from Genetic Interaction more info	PubMed
acts_upstream_of_or_within random inactivation of X chromosome	IGI Inferred from Genetic Interaction more info	PubMed
acts_upstream_of random inactivation of X chromosome	IMP Inferred from Mutant Phenotype more info	PubMed
acts_upstream_of_or_within random inactivation of X chromosome	IMP Inferred from Mutant Phenotype more info	PubMed

Component	Evidence Code	Pubs
is_active_in cellular_component	ND No biological Data available more info

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.