Official Symbol
                SLX1B-SULT1A4  provided by HGNC
 
				
                Official Full Name
				SLX1B-SULT1A4 readthrough (NMD candidate) 
                
                Gene ID
                100526831 
				
                Chromosome
                chr16
				
                Start Site
                29455105
				 
				End Site
                29464963
  
				
				Strand
                + 
  
				
				Assembly
                GRCh38
 
				
				Biotype
lncRNA 
                Also known as
- 
                
				Summary
      This locus represents naturally occurring read-through transcription between the neighboring SLX1B (SLX1 structure-specific endonuclease subunit homolog B) and SULT1A4 (sulfotransferase family, cytosolic, 1A, phenol-preferring, member 4) genes on the short arm of chromosome 16. A duplicate read-through locus also exists between the SLX1A and SULT1A3 genes located approximately 730 kb downstream on the same chromosome. 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, Feb 2017]