| GENE NAME | PLXNA3 |
| CHROMOSOME | X |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000130827 |
| UNIPROT ACCESSION NUMBER | P51805 |
| GO MOLECULAR FUNCTION | ['semaphorin receptor activity', 'protein binding'] |
| ESSENTIAL IN MOUSE | Non-essential |
| PATHWAYS | hsa04360; R-HSA-1266738; R-HSA-373755; R-HSA-399954; R-HSA-399955; R-HSA-399956; R-HSA-422475; R-HSA-9675108; hsa04360; R-HSA-1266738; R-HSA-373755; R-HSA-399954; R-HSA-399955; R-HSA-399956; R-HSA-422475; R-HSA-9675108 |
| 3 combinations linked to PLXNA3 | OLI1516; OLI1529; OLI1532 |
| 3 variants linked to PLXNA3 | PLXNA3:c.787_796del, p.Val263fs; PLXNA3:c.3944C>T, p.Pro1315Leu; PLXNA3:c.5570G>A, p.Arg1857Gln |
| 1 disease linked to PLXNA3 | 46,XY disorder of sex development |