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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. [provided by RefSeq, Dec 2012].
C21orf29; C330046G03Rik; DFNB98; ORF65; protein TSPEAR; RGD1563108; thrombospondin N-terminal domain/EPTP protein 1; thrombospondin type laminin G domain and EAR repeats; thrombospondin-type laminin G domain and EAR repeat-containing protein; thrombospondin-type laminin G domain and EAR repeats; thrombospondin-type laminin G domain and EAR repeats protein; thrombospondin-type laminin G domain and EAR repeats-containing protein; Tnep1; tspear; TSP-EAR
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