Search
Search
Bioss
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promotions']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.viewpromo']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promocode']}}: {{promo.promoCode}} {{promo.promoTitle}} {{promo.promoDescription}}. {{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.learnmore']}}
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].
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: protein TSPEAR; thrombospondin N-terminal domain/EPTP protein 1; Thrombospondin-type laminin G domain and EAR repeat-containing protein; thrombospondin-type laminin G domain and EAR repeats; thrombospondin-type laminin G domain and EAR repeats protein; thrombospondin-type laminin G domain and EAR repeats-containing protein; TSP-EAR; tspear
基因别名: C21orf29; C330046G03Rik; DFNB98; ORF65; RGD1563108; Tnep1; TSP-EAR; TSPEAR
UniProt ID: (Human) Q8WU66, (Mouse) J3S6Y1
Entrez Gene ID: (Human) 54084, (Rat) 365546, (Mouse) 252974