SG3A2 Polyclonal Antibody, 100ul Low-speed Centrifuges Mutations in this gene may

Mutations in this gene may be associated with Parkinson's disease

UNC-51-like kinase 1 and 2 (ULK1

Alternative splicing or deletion caused by a translocation event in this paternally-expressed region is responsible for Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure

GO annotations related to this gene include receptor activity and scavenger receptor activity

SG3A2 Polyclonal Antibody, 100ul Low-speed Centrifuges Mutations in this gene mayThe protein encoded by this gene is a secreted lung surfactant protein and a downstream target of thyroid transcription factor. A single nucleotide polymorphism in the promoter of this gene results in susceptibility to asthma.