基因名：
NHS
产品别名：
CTRCT40； CXN； SCML1； NHS； NHS actin remodeling regulator； NHS actin remodeling regulator； Nance-Horan syndrome protein； Nance-Horan syndrome (congenital cataracts and dental anomalies)； congenital cataracts and dental anomalies protein； 南斯-霍兰综合征蛋白；
背景信息：
This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2014]
