C330046G03Rik antibody, ORF65 antibody, TSP-EAR antibody, Tnep1 antibody, C21orf29 antibody, DFNB98 antibody, RGD1563108 antibody, thrombospondin type laminin G domain and EAR repeats antibody, thrombospondin-type laminin G domain and EAR repeats antibody, Tspear antibody, TSPEAR antibody
Background
This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants.