TSN translin [ Homo sapiens (human) ]
Source: NCBI Gene (ID 7247)
Source: NCBI Gene (ID 7247)
Symbol: TSN
Full name: translin
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: BCLF-1; C3PO; RCHF1; REHF-1; TBRBP; TRSLN
Summary: This gene encodes a DNA-binding protein which specifically recognizes conserved target sequences at the breakpoint junction of chromosomal translocations. Translin polypeptides form a multimeric structure that is responsible for its DNA-binding activity. Recombination-associated motifs and translin-binding sites are present at recombination hotspots and may serve as indicators of breakpoints in genes which are fused by translocations. These binding activities may play a crucial role in chromosomal translocation in lymphoid neoplasms. This protein encoded by this gene, when complexed with translin-associated protein X, also forms a Mg ion-dependent endoribonuclease that promotes RNA-induced silencing complex (RISC) activation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012]
Expression: Ubiquitous expression in testis (RPKM 26.5), brain (RPKM 20.8) and 25 other tissues
Orthologs: mouse
Gene size: 12203bp
Exon count: 6