GLMN Polyclonal Antibody, 20ul Peptide Library This gene encodes one of

This gene encodes one of the smaller subunits of TFIID that binds to the basal transcription factor GTF2B as well as to several transcriptional activato

and a conserved C-terminal SH2 domain

NIMA subfamily

Alstrωm syndrome

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

GLMN Polyclonal Antibody, 20ul Peptide Library This gene encodes one ofThis gene encodes a phosphorylated protein that is a member of a Skp1 Cullin F box like complex. The protein is essential for normal development of the vasculature and mutations in this gene have been associated with glomuvenous malformations, also called glomangiomas. Multiple splice variants encoding different isoforms have been found for this gene.