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SALL1基因编码的功能和结构描述

2022.8.22

该基因编码的蛋白是锌指转录抑制因子,可能是nurd组蛋白脱乙酰酶复合物(hdac)的一部分。该基因缺陷是townes-brocks综合征(tbs)和支气管耳肾综合征(bor)的病因之一。已经发现了两个编码不同亚型的转录变体。

The protein encoded by this gene is a zinc finger transcriptional repressor and may be part of the NuRD histone deacetylase complex (HDAC). Defects in this gene are a cause of Townes-Brocks syndrome (TBS) as well as bronchio-oto-renal syndrome (BOR). Two transcript variants encoding different isoforms have been found for this gene. 

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