Cytoglobin Polyclonal Antibody, 50ul Gene Synthesis Diseases associated with KCNJ16 include

Diseases associated with KCNJ16 include sesame syndrome and body dysmorphic disorder

This heterodimer binds E-box enhancer elements upstream of Period (PER1

Alternatively spliced transcript variants encoding multiple isoforms have been observed for ABCB7

This gene is a potential tumor suppressor gene that may play a role in the development of neuroblastoma

Mutations of this gene have been associated with gelatinous drop-like corneal dystrophy

Cytoglobin Polyclonal Antibody, 50ul Gene Synthesis Diseases associated with KCNJ16 includeThis gene encodes a globin protein found in vertebrate cells. The encoded protein is described as a hexacoordinate hemoglobin which binds ligand differently from the pentacoordinate hemoglobins involved in oxygen transport, and may be involved in protection during oxidative stress. This gene is located on chromosome 17 in the same region as a retinal gene which is mutated in progressive rod cone degeneration, but in the opposite orientation.