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TSPEAR

Official Full Name
thrombospondin type laminin G domain and EAR repeats
Organism
Homo sapiens
GeneID
54084
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. [provided by RefSeq, Dec 2012]
Synonyms
DFNB98; ECTD14; STHAG10; TSP-EAR; C21orf29;

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