LncRNA:ENSG00000130600

Official Symbol

H19  provided by HGNC

Official Full Name

H19 imprinted maternally expressed transcript 

Gene ID

283120 

Chromosome

chr11

Start Site

1995176

End Site

2001470

Strand

Assembly

GRCh38

Biotype

lncRNA

Also known as

ASM|ASM1|BWS|D11S813E|LINC00008|MIR675HG|NCRNA00008|WT2 

Summary

This gene is located in an imprinted region of chromosome 11 near the insulin-like growth factor 2 (IGF2) gene. This gene is only expressed from the maternally-inherited chromosome, whereas IGF2 is only expressed from the paternally-inherited chromosome. The product of this gene is a long non-coding RNA which functions as a tumor suppressor. Mutations in this gene have been associated with Beckwith-Wiedemann Syndrome and Wilms tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015] 

M6ARegulator:ENSG00000259956

Official Symbol

RBM15B  provided by HGNC

Official Full Name

RNA binding motif protein 15B 

m6A Category

writers 

Gene ID

29890 

Chromosome

chr3 

Start Site

51391285 

End Site

51397908 

Strand

Assembly

GRCh38

Biotype

protein coding 

Also known as

HUMAGCGB|HsOTT3|OTT3 

Summary

"Members of the SPEN (Split-end) family of proteins, including RBM15B, have repressor function in several signaling pathways and may bind to RNA through interaction with spliceosome components (Hiriart et al., 2005 [PubMed 16129689]).[supplied by OMIM, Feb 2009]" 

Differentially expressed Detail
Symbol H19  RBM15B 
Pvalue 3.0e-01  6.4e-01 
Log2FC 2.1e-01  -2.9e-02 
Significant NOT SIGNIFICANT  NOT SIGNIFICANT 
Correlation coefficient 0.3 
Correlation FDR 2.0e-11