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)

May be involved in neuronal NGF-dependent Ca(2+) influx

which belongs to the immunoglobulin superfamily

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

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