| GENE NAME | WNT4 |
| CHROMOSOME | 1 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000162552 |
| UNIPROT ACCESSION NUMBER | P56705 |
| GO MOLECULAR FUNCTION | ['transcription corepressor activity', 'frizzled binding', 'receptor ligand activity', 'cytokine activity'] |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa04150; hsa04310; hsa04360; hsa04390; hsa04550; hsa04916; hsa04919; hsa04934; hsa05010; hsa05022; hsa05165; hsa05200; hsa05205; hsa05217; hsa05224; hsa05225; hsa05226; R-HSA-162582; R-HSA-195721; R-HSA-201681; R-HSA-3238698; R-HSA-372790; R-HSA-373080; R-HSA-3772470; R-HSA-3858494; R-HSA-4086400; R-HSA-500792 |
| 4 combinations linked to WNT4 | OLI1141; OLI1140; OLI1231; OLI683 |
| 4 variants linked to WNT4 | WNT4:p.Val204Met; WNT4:c.739C>T, p.Arg247Cys; WNT4:c.829C>A, p.Pro277Thr; WNT4:c.896C>T, p.Thr299Met |
| 3 diseases linked to WNT4 | Holoprosencephaly; Mayer-Rokitansky-Küster-Hauser syndrome; Recurrent Pregnancy Loss |