TSPEAR 抗体
(Thrombospondin-Type Laminin G Domain and EAR Repeats (TSPEAR))
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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Latest Publications for our TSPEAR 抗体
: "Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness." in: Human molecular genetics, Vol. 21, Issue 17, pp. 3835-44, (2012) (PubMed).
Aliases for TSPEAR 抗体
thrombospondin type laminin G domain and EAR repeats (Tspear) 抗体thrombospondin type laminin G domain and EAR repeats (TSPEAR) 抗体
thrombospondin-type laminin G domain and EAR repeats (Tspear) 抗体
C21orf29 抗体
C330046G03Rik 抗体
DFNB98 抗体
ORF65 抗体
RGD1563108 抗体
Tnep1 抗体
TSP-EAR 抗体
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