LncRNA:ENSG00000261771

Official Symbol

DNAAF4-CCPG1  provided by HGNC

Official Full Name

DNAAF4-CCPG1 readthrough (NMD candidate) 

Gene ID

100533483 

Chromosome

chr15

Start Site

55355248

End Site

55498360

Strand

Assembly

GRCh38

Biotype

lncRNA

Also known as

DYX1C1-CCPG1 

Summary

This locus represents naturally occurring read-through transcription between the neighboring dyslexia susceptibility 1 candidate 1 (DYX1C1) and cell cycle progression 1 (CCPG1) genes on chromosome 15. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Mar 2011] 

M6ARegulator:ENSG00000147274

Official Symbol

RBMX  provided by HGNC

Official Full Name

RNA binding motif protein X-linked 

m6A Category

readers 

Gene ID

27316 

Chromosome

chrX 

Start Site

136848004 

End Site

136880764 

Strand

Assembly

GRCh38

Biotype

protein coding 

Also known as

HNRNPG|HNRPG|MRXS11|RBMXP1|RBMXRT|RNMX|hnRNP-G 

Summary

"This gene belongs to the RBMY gene family which includes candidate Y chromosome spermatogenesis genes. This gene, an active X chromosome homolog of the Y chromosome RBMY gene, is widely expressed whereas the RBMY gene evolved a male-specific function in spermatogenesis. Pseudogenes of this gene, found on chromosomes 1, 4, 9, 11, and 6, were likely derived by retrotransposition from the original gene. Alternatively spliced transcript variants encoding different isoforms have been identified. A snoRNA gene (SNORD61) is found in one of its introns. [provided by RefSeq, Sep 2009]" 

Differentially expressed Detail
Symbol DNAAF4-CCPG1  RBMX 
Pvalue 9.5e-12  5.0e-04 
Log2FC -2.7e+00  -2.1e-01 
Significant DOWN REGULATED  NOT SIGNIFICANT 
Correlation coefficient 0.37 
Correlation FDR 2.6e-17