| Name |
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PLXNA1 Geneplexin A1 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 positive regulation of axonogenesis. 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, Mar 2025] |
PLXNA1 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for PLXNA1 from the Pathway Commons Protein-Protein Interactions dataset. |
PLXNA1 Gene SetFrom LINCS L1000 CMAP CRISPR Knockout Consensus Signatures genes differentially expressed following the PLXNA1 gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset. |
PLXNA1 Gene SetFrom CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the PLXNA1 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas. |
PLXNA1-RANBPM complex Gene Setproteins in the PLXNA1-RANBPM complex protein complex from the CORUM Protein Complexes dataset. |
PLXNA1-related neurodevelopmental disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PLXNA1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |