Structural highlights
Disease
[SMAD9_HUMAN] Heritable pulmonary arterial hypertension. The disease may be caused by mutations affecting the gene represented in this entry.
Function
[SMAD9_HUMAN] Transcriptional modulator activated by BMP (bone morphogenetic proteins) type 1 receptor kinase. SMAD9 is a receptor-regulated SMAD (R-SMAD).