XRN2 Polyclonal Antibody, 50ul Measuring Instruments Several alternatively spliced transcript variants

Several alternatively spliced transcript variants encoding a few distinct isoforms have been reported

Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss

or Transcription factor 12 (on chromosome 15)

Also interacts with MAP3K8

GO annotations related to this gene include enzyme binding and RNA polymerase II transcription corepressor activity

XRN2 Polyclonal Antibody, 50ul Measuring Instruments Several alternatively spliced transcript variantsXRN2 encodes a 5' 3' exonuclease that promotes transcription termination at cotranscriptional cleavage sites. Alternative splicing results in multiple transcript variants encoding different isoforms.