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

The encoded protein functions as a subunit of the tuberous sclerosis TSC1-TSC2 complex which plays a role in the regulation of cellular growth and differentiation

sequence Wrong choice of CDS

These proteins are associated with pre-mRNAs in the nucleus and regulate alternative splicing

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.