PLXNA1 Chromosome 3

Plexin A1
20 variants 20 Health Risk

Upload your DNA to see your personal genotypes for variants in PLXNA1.

What This Gene Does
Predicted to enable semaphorin receptor activity. Predicted to be involved in several processes, including T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell; nervous system development; and semaphorin-plexin signaling pathway. Predicted to act upstream of or within dichotomous subdivision of terminal units involved in salivary gland branching; neuron projection extension; and regulation of smooth muscle cell migration. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Gene Info
Gene Group
"Plexins|IPT domain containing"
Locus Type
gene with protein product
Location
3q21.3
Ensembl
ENSG00000114554
Associated Conditions (4)
PLXNA1-related disorder
Neurodevelopmental disorder
Dworschak-Punetha neurodevelopmental syndrome
Neurodevelopmental disorder with variable cerebral and eye anomalies
Key Variants
All Variants (20)
RSID Category Clinical Significance Conditions
RS138276286 Health Risk Conflicting classifications of pathogenicity PLXNA1-related disorder, PLXNA1-related disorder
RS199523740 Health Risk Conflicting classifications of pathogenicity PLXNA1-related disorder, PLXNA1-related disorder
RS200374384 Health Risk Conflicting classifications of pathogenicity PLXNA1-related disorder, PLXNA1-related disorder
RS2079185551 Health Risk Conflicting classifications of pathogenicity Neurodevelopmental disorder, PLXNA1-related disorder, Neurodevelopmental disorder
RS370434411 Health Risk Conflicting classifications of pathogenicity PLXNA1-related disorder, PLXNA1-related disorder
RS375833812 Health Risk Conflicting classifications of pathogenicity Neurodevelopmental disorder, PLXNA1-related disorder, Neurodevelopmental disorder
RS377693045 Health Risk Conflicting classifications of pathogenicity
RS557203949 Health Risk Conflicting classifications of pathogenicity Dworschak-Punetha neurodevelopmental syndrome, Dworschak-Punetha neurodevelopmental syndrome
RS747148568 Health Risk Conflicting classifications of pathogenicity
RS772360004 Health Risk Conflicting classifications of pathogenicity Dworschak-Punetha neurodevelopmental syndrome, PLXNA1-related disorder, Dworschak-Punetha neurodevelopmental syndrome
RS1394805238 Health Risk Likely pathogenic
RS2079215968 Health Risk Likely pathogenic Neurodevelopmental disorder, Neurodevelopmental disorder
RS2107620082 Health Risk Likely pathogenic Neurodevelopmental disorder, Dworschak-Punetha neurodevelopmental syndrome, Neurodevelopmental disorder
RS2472529640 Health Risk Likely pathogenic Neurodevelopmental disorder with variable cerebral and eye anomalies, Neurodevelopmental disorder with variable cerebral and eye anomalies
RS2472529689 Health Risk Likely pathogenic Dworschak-Punetha neurodevelopmental syndrome, Dworschak-Punetha neurodevelopmental syndrome
RS2107631669 Health Risk Pathogenic
RS766352439 Health Risk Pathogenic
RS1204647586 Health Risk Pathogenic/Likely pathogenic Neurodevelopmental disorder, Dworschak-Punetha neurodevelopmental syndrome, PLXNA1-related disorder
RS2079056783 Health Risk Pathogenic/Likely pathogenic Neurodevelopmental disorder, Dworschak-Punetha neurodevelopmental syndrome, Neurodevelopmental disorder
RS2079109807 Health Risk Pathogenic/Likely pathogenic Neurodevelopmental disorder, Dworschak-Punetha neurodevelopmental syndrome, Neurodevelopmental disorder
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