这个基因是一个系统学保守的基因家族的成员,该家族共享一个共同的DNA结合域T-boxT-box基因编码参与发育过程调控的转录因子该基因突变与遗传性x连锁疾病(腭裂伴舌苔强直)有关,并被认为在人类腭裂发生中起主要作用。另外,已经发现该基因编码不同亚型的剪接转录变体[由RefSeq提供,2008年7月]
This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

基因名:TBX22
别名:CPX,CLPA,TBXX,ABERS,dJ795G23.1
基因ID:50945
Chromosome:
(GRCh37)
X Start: 79270255 End: 79287268 Strand: 
信号通路:  
TBX22 基因突变与药物

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