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TSPEAR


Official Full Name
thrombospondin type laminin G domain and EAR repeats
Organism
Homo sapiens
Gene ID
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

Cat.No. Product Name Price
SHH436452 shRNA set against Human TSPEAR (NM_144991.2) Inquiry
Cat.No. Product Name Price
CDCR317975 Human TSPEAR ORF Clone(NM_144991.2) Inquiry
CDFG008790 Human TSPEAR cDNA Clone(NM_144991.2) Inquiry
MiUTR1H-01341 TSPEAR miRNA 3'UTR clone Inquiry
CDCB190592 Rabbit TSPEAR ORF clone (XM_008252306.1) Inquiry
CDCS419870 Human TSPEAR ORF Clone (BC021197) Inquiry
CDCS419871 Human TSPEAR ORF Clone (BC115415) Inquiry
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