GNL1 Polyclonal Antibody, 100ul Hepatocytes Mutations and deletions in this

Mutations and deletions in this gene are associated with benign hereditary chorea| choreoathetosis| congenital hypothyroidism| and neonatal respiratory distress| and may be associated with thyroid cancer

A frequent polymorphism in the translation start codon of this gene can abolish translation and may be associated with forms of deafness

a major risk factor for coronary artery disease

NAB2 encodes a member of the family of NGFI-A binding (NAB) proteins

GNL1 Polyclonal Antibody, 100ul Hepatocytes Mutations and deletions in thisThe GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA E, in the same transcriptional orientation. GNL1 is telomeric to HLA B and HLA C.