该基因编码fanconi贫血补体b组的一个成员。该蛋白被组装成一个核蛋白复合物，参与dna损伤的修复。该基因突变可导致染色体不稳定和脑积水的Vacterl综合征。[由RefSeq提供，2016年4月]
This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
| 基因名： | FANCB |
| 别名： | FA2,FAB,FACB,FAAP90,FAAP95 |
| 基因ID： | 2187 |
| Chromosome： (GRCh37) | X Start: 14861529 End: 14891184 Strand: |
| 信号通路： |
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