STK33 Polyclonal Antibody, 50ul Cell Culture Flasks Mutations in this gene cause

Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome

a congenital defect of the anterior chamber of the eye

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with bacteriocidal activity against S

The protein encoded by LEPR belongs to the gp130 family of cytokine receptors that are known to stimulate gene transcription via activation of cytosolic STAT proteins

STK33 Polyclonal Antibody, 50ul Cell Culture Flasks Mutations in this gene causeSTK33 (Serine Threonine Kinase 33) is a Protein Coding gene. Among its related pathways are Sweet Taste Signaling. Gene Ontology (GO) annotations related to this gene include transferase activity, transferring phosphorus containing groups and protein tyrosine kinase activity. An important paralog of this gene is DCX. Serine threonine protein kinase which phosphorylates VIME. May play a specific role in the dynamic behavior of the intermediate filament