NRP2 Chromosome 2

Neuropilin 2
2 variants 2 Health Risk

Upload your DNA to see your personal genotypes for variants in NRP2.

What This Gene Does
This gene encodes a member of the neuropilin family of receptor proteins. The encoded transmembrane protein binds to SEMA3C protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C} and SEMA3F protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F}, and interacts with vascular endothelial growth factor (VEGF). This protein may play a role in cardiovascular development, axon guidance, and tumorigenesis. This protein has also been determined to act as a co-receptor for SARS-CoV-2 (which causes COVID-19) to infect host cells. [provided by RefSeq, Jul 2021]
Associated Conditions (2)
NRP2-related disorder
Inborn genetic diseases
Key Variants
All Variants (2)
RSID Category Clinical Significance Conditions
RS910717989 Health Risk Conflicting classifications of pathogenicity NRP2-related disorder, NRP2-related disorder
RS779617179 Health Risk Likely pathogenic Inborn genetic diseases, NRP2-related disorder, Inborn genetic diseases
Sign Up to Analyze Your DNA Log In