蛋白质/抗原/多肽 >> 重组蛋白
重组SHFM3蛋白
半岛bd体育手机客户端 介绍
基因名：
FBXW4 半岛bd体育手机客户端 别名： DAC； FBW4； FBWD4； SHFM3； SHSF3； FBXW4； F-box and WD repeat domain containing 4； F-box and WD repeat domain containing 4； F-box/WD repeat-containing protein 4； F-box and WD-40 domain protein 4； F-box and WD-40 domain-containing protein 4； F-box/WD repeat protein 4； dactylin； epididymis secretory sperm binding protein； SHFM3蛋白； 背景信息：
Probably recognizes and binds to some phosphorylated proteins and promotes their ubiquitination and degradation. Likely to be involved in key signaling pathways crucial for normal limb development. May participate in Wnt signaling.
Involvement in disease:Defects in FBXW4 are a cause of split-hand/foot malformation type 3 (SHFM3) . SHFM3 is an autosomal dominant disorder characterized by hypoplasia/aplasia of the central digits with fusion of the remaining digits. 标签：His-tag |
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