该基因编码c2h2型锌指蛋白zic家族的一个成员。这种核蛋白在左右体轴形成的早期可能起转录因子的作用。该基因的突变导致X连锁内脏异位，包括先天性心脏病和器官中的左右轴缺陷。[由RefSeq提供，2008年7月]
This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. This nuclear protein probably functions as a transcription factor in early stages of left-right body axis formation. Mutations in this gene cause X-linked visceral heterotaxy, which includes congenital heart disease and left-right axis defects in organs. [provided by RefSeq, Jul 2008]
| 基因名： | ZIC3 |
| 别名： | HTX,HTX1,ZNF203,VACTERLX |
| 基因ID： | 7547 |
| Chromosome： (GRCh37) | X Start: 136648346 End: 136654259 Strand: |
| 信号通路： |
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