KIR5.1(Phospho Ser416) Polyclonal Antibody, 100ul Enzymes 5-trisphosphate to 1

5-trisphosphate to 1

Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes

Mutations in PARK2 are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease

|Contains 1 bZIP domain

KIR5.1(Phospho Ser416) Polyclonal Antibody, 100ul Enzymes 5-trisphosphate to 1KCNJ16 (Potassium Voltage Gated Channel Subfamily J Member 16) is a Protein Coding gene. Diseases associated with KCNJ16 include sesame syndrome and body dysmorphic disorder. Among its related pathways are Transmission across Chemical Synapses and Inwardly rectifying K+ channels. GO annotations related to this gene include inward rectifier potassium channel activity. An important paralog of this gene is KCNJ3. nward rectifier potassium channels are