HMGA2 Polyclonal Antibody, 50ul NGS Oligos craniofacial-deafness-hand syndrome

craniofacial-deafness-hand syndrome

are integral transmembrane proteins that exchange extracellular Na+ for intracellular H+

It is proposed that this gene plays a role in mitochondrial protein metabolism and could be involved in mitochondrial pathologies

The function of the encoded protein is not known

HMGA2 Polyclonal Antibody, 50ul NGS Oligos craniofacial-deafness-hand syndromeThis gene encodes a protein that belongs to the non histone chromosomal high mobility group (HMG) protein family. HMG proteins function as architectural factors and are essential components of the enhancesome. This protein contains structural DNA binding domains and may act as a transcriptional regulating factor. Identification of the deletion, amplification, and rearrangement of this gene that are associated with myxoid liposarcoma suggests a role in