FXYD4 Rabbit Polyclonal Antibody, 20ul Digital Burette Defects in this gene are

Defects in this gene are associated with Charcot-Marie-Tooth disease type 1D (CMT1D)

including membrane receptor signaling

Forming a subgroup of the HMG domain superfamily

MIM 113508) when phosphorylated (Kovacina et al

Structural analysis of the protein suggests that Annexin VII is a membrane binding protein with diverse properties

FXYD4 Rabbit Polyclonal Antibody, 20ul Digital Burette Defects in this gene areThis gene encodes a member of a family of small membrane proteins that share a 35 amino acid signature sequence domain beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. The approved human gene nomenclature for the family is FXYD domain containing ion transport regulator. FXYD4 originally named CHIF for channel inducing factor has been shown to modulate the properties of the Na K ATPase as has FXYD2 also