XRN2 Polyclonal Antibody, 50ul Measuring Instruments and one finding suggests that

and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism

This gene is located in a region on chromosome X

several dominant human NOG mutations in unrelated families with proximal symphalangism (SYM1) and mu

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

Also interacts with MAP3K8

XRN2 Polyclonal Antibody, 50ul Measuring Instruments and one finding suggests thatXRN2 encodes a 5' 3' exonuclease that promotes transcription termination at cotranscriptional cleavage sites. Alternative splicing results in multiple transcript variants encoding different isoforms.