| GENE NAME | WNT9A |
| CHROMOSOME | 1 |
| ENSEMBL ID | ENSG00000143816 |
| ENTREZ ID | 7483 |
| UNIPROT ACCESSION NUMBER | O14904 |
| GO MOLECULAR FUNCTION | protein binding; signaling receptor binding; cytokine activity; frizzled binding; receptor ligand activity |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa05224; hsa05205; R-HSA-3772470; hsa05010; hsa04916; hsa05022; R-HSA-201681; hsa05200; hsa05226; hsa05217; hsa05225; hsa04310; hsa04390; hsa05205; hsa05010; hsa04150; hsa04934; hsa05224; hsa04550; hsa05165; R-HSA-500792; hsa05217; hsa04310; R-HSA-195721; R-HSA-373080; hsa05225; R-HSA-162582; R-HSA-372790; hsa04916; hsa05022; R-HSA-3238698; hsa05226; hsa05200; hsa04934; hsa04150; hsa04550; hsa05165; hsa04390 |
| 4 combinations linked to WNT9A | OLI693; OLI604; OLI721; OLI348 |
| 3 variants linked to WNT9A | WNT9A:c.353-30G>A, ; WNT9A:c.1070G>A, p.Arg357His; WNT9A:c.998G>A, p.Arg333Gln |
| 3 diseases linked to WNT9A | Isolated anencephaly; Disorder of sex development; 46,XY disorder of sex development |