ATG9B Polyclonal Antibody, 50ul Centrifuges Defects in this gene are

Defects in this gene are a cause of familial amyloidosis Finnish type (FAF)

two other members of the DEAD box protein family

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May interact with SBDS

A missense mutation in this gene is associated with hypokalemic periodic paralysis

ATG9B Polyclonal Antibody, 50ul Centrifuges Defects in this gene areThis gene functions in the regulation of autophagy, a lysosomal degradation pathway. This gene also functions as an antisense transcript in the posttranscriptional regulation of the endothelial nitric oxide synthase 3 gene, which has 3' overlap with this gene on the opposite strand. Mutations in this gene and disruption of the autophagy process have been associated with multiple cancers. Alternative splicing results in multiple transcript variants.