AAA1 Polyclonal Antibody, 20ul Aspirating Pipets Mutations in this gene are

Mutations in this gene are associated with a variety of human cancers| including hereditary cancers such as Li-Fraumeni syndrome

A pseudogene of this gene is also present on chromosome 5

The synergy of this protein and the APP is required to mediate neuromuscular transmission

GPR37L1 (G Protein-Coupled Receptor 37 Like 1) is a Protein Coding gene

Mutations in this gene cause X-linked agammaglobulinemia type 1| which is an immunodeficiency characterized by the failure to produce mature B lymphocytes| and associated with a failure of Ig heavy chain rearrangement

AAA1 Polyclonal Antibody, 20ul Aspirating Pipets Mutations in this gene areSLC7A10 in association with 4F2HC (SLC3A2; MIM 158070) mediates high affinity transport of D serine and several other neutral amino acids (Nakauchi et al. 2000