KEGG   VARIANT: 7480v1
Entry
7480v1                      Variant                                
Name
WNT10B mutation
Type
Loss of function
Gene
WNT10B  Wnt family member 10B [KO:K01357]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 601906
Network
nt06505  WNT signaling
Disease
H00471  Split-hand/foot malformation
H00625  Tooth agenesis
Reference
  Authors
Yu M, Wong SW, Han D, Cai T
  Title
Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
  Journal
Oral Dis 25:646-651 (2019)
DOI:10.1111/odi.12931
Reference
  Authors
Martinez-Gil N, Ugartondo N, Grinberg D, Balcells S
  Title
Wnt Pathway Extracellular Components and Their Essential Roles in Bone Homeostasis.
  Journal
Genes (Basel) 13:138 (2022)
DOI:10.3390/genes13010138
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