人 TSPEAR (NM_144991) cDNA克隆

Accession: NM_144991
基因名称: TSPEAR
基因别名: DFNB98; TSP-EAR; C21orf29
基因描述: Homo sapiens thrombospondin-type laminin G domain and EAR repeats (TSPEAR), transcript variant 1, mRNA.
种属: Human
CDS区长度: 2010 (查看编码区序列)
翻译后氨基酸长度: 669 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longer isoform (1).
产品编号 产品名称 载体 规格 价格
G112047 人 TSPEAR (NM_144991) cDNA克隆 pDONR223 2ug质粒 点击询价

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]