Tissue expression
Cell line expression
Protein structure
TSPEAR
Thrombospondin type laminin G domain and EAR repeatsC21orf29, DFNB98, MGC11251, TSP-EAR
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]
Top validated antibodies |
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antibodies-online | ![]() |
2 references | Polyclonal |
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Aviva Systems Biology | ![]() |
Polyclonal |
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OriGene | ![]() |
Polyclonal |
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GeneTex | ![]() |
Polyclonal |
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Invitrogen Antibodies | ![]() |
Polyclonal |
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