XRN2 Polyclonal Antibody, 50ul Measuring Instruments Defects in this gene likely

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

This gene is located in a region on chromosome X

This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations

Equipped with a 0

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

XRN2 Polyclonal Antibody, 50ul Measuring Instruments Defects in this gene likelyXRN2 encodes a 5' 3' exonuclease that promotes transcription termination at cotranscriptional cleavage sites. Alternative splicing results in multiple transcript variants encoding different isoforms.