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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].
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Protein Aliases: protein TSPEAR; thrombospondin N-terminal domain/EPTP protein 1; 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; TSP-EAR; tspear
Gene Aliases: C21orf29; C330046G03Rik; DFNB98; ORF65; RGD1563108; Tnep1; TSP-EAR; TSPEAR
UniProt ID: (Human) Q8WU66, (Mouse) J3S6Y1
Entrez Gene ID: (Human) 54084, (Rat) 365546, (Mouse) 252974
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