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TSPEAR is 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.
Gene Name: | Thrombospondin-type laminin G domain and EAR repeats |
Synonyms: | TSPEAR |
Target Sequences: | NM_144991 NP_659428.2 |
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