Human Wnt genes
There is a separate table for syntenic linkage groups. See the comparative table of all vertebrate Wnt genes for and explanation of the numbering/nomenclature. Also, see alignments of Wnt proteins
Link to OMIM | Linked to HUGO |
Disease |
WNT1 | Osteogenesis imperfecta Fahiminiya et al, 2013
|
|
WNT2 | ||
WNT3 | WNT3 | Tetra-Amelia (Niemann 2004) |
WNT3A | WNT3A | |
WNT4 | WNT4 | Mullerian-duct
regression and virilization (Biason-Lauber
2004)
SERKAL syndrome (Mandel, 2008) |
WNT5A | WNT5A | Robinow syndrome (Person 2010) |
WNT5B | WNT5B | Associated with Susceptibility to type 2 diabetes (Kanazawa 2004) |
WNT6 | WNT6 | |
WNT7A | WNT7A | Fuhrmann syndrome |
WNT7B | WNT7B | |
WNT8B | WNT8B | |
WNT9A | WNT9A
|
|
WNT9B | WNT9B | |
WNT10A | WNT10A | Odonto-onycho-dermal dysplasia Adaimy, 2007 , Bohring, 2009 |
WNT10B | WNT10B | Mutations in
Obesity patients Christodoulides
2006
Split-Hand/Foot Malformation (Ugur 2008) |
WNT11 | WNT11 | |
WNT16 | WNT16 | Bone density (Zheng et al, 2012) |