2 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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13PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingnegative regulation of BMP signaling pathwayAMPA glutamate receptor complexGO:0005615alcohol drinkingmathematical abilityinsomniametabolic syndrome
Based on limited published evidence, VWC2L (von Willebrand factor C domain containing 2 like) is a secreted cysteine knot protein that modulates bone and neural development. In osteoblasts, VWC2L accelerates matrix mineralization and increases Osterix expression, likely through TGF-β superfamily signaling 1. As a BMP antagonist of the Chordin family, VWC2L weakly inhibits BMP activity and promotes neurogenesis in neural precursor cells 2. The protein is expressed in brain tissue and ubiquitously across other tissues. VWC2L's functions align with its annotation for negative regulation of BMP signaling and involvement in neurogenesis and bone differentiation.
1
VWC2L promotes matrix mineralization in osteoblasts by increasing Osterix expression through TGF-β signaling pathway
PMID: 222098472
VWC2L (Brorin-like) is a BMP antagonist that promotes neurogenesis in neural precursor cells and is predominantly expressed in brain
PMID: 19852960⚠Limited data available — This gene has 2 indexed publications. Summary and analysis may be incomplete.
alcohol drinkingOpen Targets
mathematical abilityOpen Targets
metabolic syndromeOpen Targets
neurotic disorderOpen Targets
liver diseaseOpen Targets
nervous system diseaseOpen Targets
Myasthenia gravisOpen Targets
adolescent idiopathic scoliosisOpen Targets
chronic intestinal vascular insufficiencyOpen Targets
attention deficit hyperactivity disorderOpen Targets
diabetic ketoacidosisOpen Targets
Herpes ZosterOpen Targets
Benign Thyroid Gland NeoplasmOpen Targets
autism spectrum disorderOpen Targets
ocular hypotensionOpen Targets
placenta praeviaOpen Targets
nutritional deficiency diseaseOpen Targets
No pathogenic variants reported on ClinVar for this gene.