rs763112634
This variant is located in the LTBP4 gene.
▶ClinVar annotation
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies; not provided
View on ClinVar →About LTBP4
The protein encoded by this gene binds transforming growth factor beta (TGFB) as it is secreted and targeted to the extracellular matrix. TGFB is biologically latent after secretion and insertion into the extracellular matrix, and sheds TGFB and other proteins upon activation. Defects in this gene may be a cause of cutis laxa and severe pulmonary, gastrointestinal, and urinary abnormalities. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]
View all LTBP4 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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