分子量：Calculated MW: 11kDa/16kDa/34kDa
Observed MW: 37kDa

细胞定位：Nucleus

稀释方法：WB 1:500 - 1:2000
IF 1:50 - 1:200

总结：This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.