TTYH2 Rabbit Polyclonal Antibody, 20ul Human Genome Knockout Libraries Diseases associated with GPR176 include

Diseases associated with GPR176 include waterhouse-friderichsen syndrome

There are at least two protein isoforms of the Double C2 protein| namely alpha (DOC2A) and beta (DOC2B)| which contain two C2-like domains

Defects in this gene are the cause of glycogen storage disease II| also known as Pompe's disease| which is an autosomal recessive disorder with a broad clinical spectrum

Proteolysis also occurs by way of CUL-4 associating with Nedd-8

TTYH2 Rabbit Polyclonal Antibody, 20ul Human Genome Knockout Libraries Diseases associated with GPR176 includeThis gene encodes a member of the tweety family of proteins. Members of this family function as chloride anion channels. The encoded protein functions as a calcium(2+) activated large conductance chloride( ) channel and may play a role in kidney tumorigenesis. Two transcript variants encoding distinct isoforms have been identified for this gene.