SYFM Rabbit Polyclonal Antibody, 50ul Cell fragmentation and collection SNF1 subfamily

SNF1 subfamily

Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder

synaptojanin

Activated by diacylglycerol (DAG) (By similarity)

The encoded protein functions in part by phosphorylating members of the mitotic checkpoint complex and activating the spindle checkpoint

SYFM Rabbit Polyclonal Antibody, 50ul Cell fragmentation and collection SNF1 subfamilyThis gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants.