C330046G03Rik antikoerper, ORF65 antikoerper, TSP-EAR antikoerper, Tnep1 antikoerper, C21orf29 antikoerper, DFNB98 antikoerper, RGD1563108 antikoerper, thrombospondin type laminin G domain and EAR repeats antikoerper, thrombospondin-type laminin G domain and EAR repeats antikoerper, Tspear antikoerper, TSPEAR antikoerper
Hintergrund
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.