ROR Gamma Polyclonal Antibody, 20ul Centrifuge Tube (Bottle) Mutations in this gene are

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

Four transcript variants that produce four isoforms of the calcium/calmodulin dependent enzyme have been identified as well as two transcripts that produce two isoforms of telokin

The encoded protein is known to play a role in cystic fibrosis and Huntington's disease

The cleavage of p35 into p25 results in relocalization of the protein from the cell periphery to nuclear and perinuclear regions

which belongs to the immunoglobulin superfamily

ROR Gamma Polyclonal Antibody, 20ul Centrifuge Tube (Bottle) Mutations in this gene areNuclear receptor ROR gamma encoded by this gene is a DNA binding transcription factor and is a member of the NR1 subfamily of nuclear hormone receptors. The specific functions of this protein are not known; however, studies of a similar gene in mice have shown that this gene may be essential for lymphoid organogenesis and may play an important regulatory role in thymopoiesis. In addition, studies in mice suggest that the protein encoded by this gene