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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TSPEAR-20-RE | 20 (40 μL) | 200 μL |  |
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| TSPEAR-20-OR | 20 (40 μL) | 200 μL |  |
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| TSPEAR-20-GO | 20 (40 μL) | 200 μL |  |
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| TSPEAR-20-GR | 20 (40 μL) | 200 μL |  |
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| TSPEAR-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : TSPEAR
Gene Name : Thrombospondin type laminin G domain and EAR repeats
Chromosome : CHR 21: 447,115,79-444,978,91
Locus : 21q22.3
Alt. Genes : LRPPRC
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