S26A4 Polyclonal Antibody, 100ul Mammalian Expression Several human genetic disorders are

Several human genetic disorders are caused by aberrations in human homeobox genes

tissue specificity:Seems to be expressed in prostate and less abundantly in adult brain

2001 [PubMed 11689425])

May play a role in the trafficking of activated/effector T-lymphocytes to inflammatory sites and other aspects of activated T-lymphocyte physiology

with a role in targeting this protein to chromatin during anaphase

S26A4 Polyclonal Antibody, 100ul Mammalian Expression Several human genetic disorders areMutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.