SPEG Polyclonal Antibody, 20ul Organelle Studies EPHA7 belongs to the ephrin

EPHA7 belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family

Remote control panel prevents manual disturbance during operation

Alterations of this gene| including point mutations| insertions and deletions| cause factor IX deficiency| which is a recessive X-linked disorder| also called hemophilia B or Christmas disease

|Belongs to the histone deacetylase family

frontometaphyseal dysplasia (FMD)

SPEG Polyclonal Antibody, 20ul Organelle Studies EPHA7 belongs to the ephrinThis gene encodes a protein with similarity to members of the myosin light chain kinase family. This protein family is required for myocyte cytoskeletal development. Along with the desmin gene, expression of this gene may be controlled by the desmin locus control region. Mutations in this gene are associated with centronuclear myopathy 5.