EZH2 Polyclonal Antibody, 100ul DNA Oligo Synthesis Mutations in NT5C3A are a

Mutations in NT5C3A are a cause of hemolytic anemia due to uridine 5-prime monophosphate hydrolase deficiency

This gene encodes a protein which contains a domain found in an AT-hook-containing transcription factor

subunit:Interacts with cul3

Mutations in this gene have been associated with mitochondrial neurogastrointestinal encephalomyopathy

with homology to gp130

EZH2 Polyclonal Antibody, 100ul DNA Oligo Synthesis Mutations in NT5C3A are aThis gene encodes a member of the Polycomb group (PcG) family. PcG family members form multimeric protein complexes, which are involved in maintaining the transcriptional repressive state of genes over successive cell generations. This protein associates with the embryonic ectoderm development protein, the VAV1 oncoprotein, and the X linked nuclear protein. This protein may play a role in the hematopoietic and central nervous systems. Multiple