ULK4 Polyclonal Antibody, 100ul Enzyme Activity Assays Mutations in this gene are

Mutations in this gene are associated with hypochromic microcytic anemia with iron overload

CCAAT/enhancer binding protein beta functions as a homodimer but can also form heterodimers with CCAAT/enhancer-binding proteins alpha

and the ephrin-B (EFNB) class

DUF1220 copy number variations in human chromosomal region 1q21

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ULK4 Polyclonal Antibody, 100ul Enzyme Activity Assays Mutations in this gene areThis gene encodes a member of the unc 51 like serine threonine kinase (STK) family. Members of this protein family play a role in neuronal growth and endocytosis. The encoded protein is likely involved in neurite branching, neurite elongation and neuronal migration. Genome wide association studies (GWAS) indicate an association of variations in this gene with blood pressure and hypertension. Sequence variations in this gene may also be be associated