UBP14 Polyclonal Antibody, 50ul Cell Separation and Collection Diseases associated with GPR176 include

Diseases associated with GPR176 include waterhouse-friderichsen syndrome

Three transcript variants encoding different isoforms have been found for SP1

This gene encodes the e subunit of the Fo complex

There are multiple pseudogenes of this gene dispersed throughout the genome

The serine/threonine-protein kinase tousled-like 2 is thought to function in the regulation of chromatin assembly in the S phase of the cell cycle by regulating the levels of a histone H3/H4 chaperone

UBP14 Polyclonal Antibody, 50ul Cell Separation and Collection Diseases associated with GPR176 includeThis gene encodes a member of the ubiquitin specific processing (UBP) family of proteases that is a deubiquitinating enzyme (DUB) with His and Cys domains. This protein is located in the cytoplasm and cleaves the ubiquitin moiety from ubiquitin fused precursors and ubiquitinylated proteins. Mice with a mutation that results in reduced expression of the ortholog of this protein are retarded for growth, develop severe tremors by 2 to 3 weeks of age