NEGR1 Polyclonal Antibody, 100ul Micro Centrifuge Tubes Defects in this gene are

Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome

Uniform thickness of the bottom of the plate

the TRAF domain

which belongs to the seven-transmembrane-domain G protein-coupled receptor (GPCR) superfamily

Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3)

NEGR1 Polyclonal Antibody, 100ul Micro Centrifuge Tubes Defects in this gene areNEGR1 is a Protein Coding gene. Diseases associated with NEGR1 include podoconiosis. Among its related pathways are Cell adhesion molecules (CAMs). An important paralog of this gene is LSAMP. May be involved in cell adhesion. May function as a trans neural growth promoting factor in regenerative axon sprouting in the mammalian brain.