TFII-I(Phospho Tyr248) Polyclonal Antibody, 20ul Antisense Oligonucleotides Defects in SIX1 are a

Defects in SIX1 are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3)

and RPH3A is a RAB3A effector (Lin et al

Actinin alpha 3 (gene/pseudogene) is primarily expressed in skeletal muscle and functions as a structural component of sarcomeric Z line

human immunodeficiency virus type 1 (HIV-1) and vesicular stomatitis virus (VSV)

a congenital defect of the anterior chamber of the eye

TFII-I(Phospho Tyr248) Polyclonal Antibody, 20ul Antisense Oligonucleotides Defects in SIX1 are aThis gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21.