rs149015682
This variant is located in the SMAD9 gene.
▶ClinVar annotation
Uncertain Significance★★★☆
3 submitters2 publicationsPulmonary hypertension, primary, 2; SMAD9-related disorder; not provided
View on ClinVar →About SMAD9
The protein encoded by this gene is a member of the SMAD family, which transduces signals from TGF-beta family members. The encoded protein is activated by bone morphogenetic proteins and interacts with SMAD4. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010]
View all SMAD9 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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