| GENE NAME | WNT9B |
| CHROMOSOME | 17 |
| ENSEMBL ID | ENSG00000158955 |
| ENTREZ ID | 7484 |
| UNIPROT ACCESSION NUMBER | O14905 |
| GO MOLECULAR FUNCTION | frizzled binding; cytokine activity; receptor ligand activity; co-receptor binding |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa04310; R-HSA-195721; R-HSA-373080; R-HSA-162582; R-HSA-372790; R-HSA-500792; hsa05200; hsa04916; hsa05022; hsa05217; R-HSA-3238698; hsa05224; hsa04150; hsa05205; hsa05010; hsa04550; hsa05165; hsa04390; hsa04934; hsa05226; hsa05225 |
| 6 combinations linked to WNT9B | OLI604; OLI1144; OLI344; OLI028; OLI351; OLI027 |
| 6 variants linked to WNT9B | WNT9B:c.6dupC, p.Arg2fsTer55; WNT9B:c.973C>T, p.Arg325Cys; WNT9B:c.*158C>T, None; WNT9B:c.1059C>T, p.Tyr353=; WNT9B:c.134C>T, p.Pro45Leu; WNT9B:c.454G>A, p.Glu152Lys |
| 4 diseases linked to WNT9B | Müllerian aplasia; Disorder of sex development; Mayer-Rokitansky-Küster-Hauser syndrome; 46,XY disorder of sex development |