TM59L Rabbit Polyclonal Antibody, 20ul Thermal Control Mutations in the gene cause

Mutations in the gene cause Sjogren-Larsson syndrome

which is found in high concentrations in biological fluids and is expressed in virtually all organs of the body

The protein encoded by ATG16L1 (autophagy related 16 like 1) is part of a large protein complex that is necessary for autophagy

TBX3 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain

LIM domain kinase 1 also stimulates axon growth and may play a role in brain development

TM59L Rabbit Polyclonal Antibody, 20ul Thermal Control Mutations in the gene causeThis gene encodes a predicted type I membrane glycoprotein. The encoded protein may play a role in functioning of the central nervous system.