XRN2 Polyclonal Antibody, 50ul Measuring Instruments several dominant human NOG mutations

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

This gene is located in a region on chromosome X

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

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

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

XRN2 Polyclonal Antibody, 50ul Measuring Instruments several dominant human NOG mutationsXRN2 encodes a 5' 3' exonuclease that promotes transcription termination at cotranscriptional cleavage sites. Alternative splicing results in multiple transcript variants encoding different isoforms.