SCUBE3 Chromosome 6

Signal peptide, CUB domain and EGF like domain containing 3
9 variants 9 Health Risk

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What This Gene Does
This gene encodes a member of the signal peptide, complement subcomponents C1r/C1s, Uegf, bone morphogenetic protein-1 and epidermal growth factor-like domain containing protein family. Overexpression of this gene in human embryonic kidney cells results in secretion of a glycosylated form of the protein that forms oligomers and tethers to the cell surface. This gene is upregulated in lung cancer tumor tissue compared to healthy tissue and is associated with loss of the epithelial marker E-cadherin and with increased expression of vimentin, a mesenchymal marker. In addition, the protein encoded by this gene is a transforming growth factor beta receptor ligand, and when secreted by cancer cells, it can be cleaved in vitro to release the N-terminal epidermal growth factor-like repeat domain and the C-terminal complement subcomponents C1r/C1s domain. Both the full length protein and C-terminal fragment can bind to the transforming growth factor beta type II receptor to promote the epithelial-mesenchymal transition and tumor angiogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
Associated Conditions (7)
Abnormality of the dentition
Abnormal facial shape
Short stature
Abnormality of the skeletal system
facial dysmorphism
and skeletal anomalies with or without cardiac anomalies 2
Inborn genetic diseases
Key Variants
All Variants (9)
RSID Category Clinical Significance Conditions
RS1436996181 Health Risk Conflicting classifications of pathogenicity Abnormality of the dentition, Abnormal facial shape, Short stature
RS61745528 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1397172310 Health Risk Pathogenic Abnormality of the dentition, Abnormal facial shape, Short stature
RS1783419625 Health Risk Pathogenic Abnormality of the dentition, Abnormal facial shape, Short stature
RS1783620400 Health Risk Pathogenic Abnormality of the dentition, Abnormal facial shape, Short stature
RS1784124318 Health Risk Pathogenic
RS1784221557 Health Risk Pathogenic Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2
RS1784291936 Health Risk Pathogenic Abnormality of the dentition, Abnormal facial shape, Short stature
RS751478115 Health Risk Pathogenic/Likely pathogenic Abnormality of the dentition, Abnormal facial shape, Short stature
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