KEGG   VARIANT: 7476v1
Entry
7476v1                      Variant                                
Name
WNT7A mutation
Type
Loss of function
Gene
WNT7A  Wnt family member 7A [KO:K00572]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 601570
Network
nt06505  WNT signaling
Disease
H00846  Fuhrmann syndrome
H00847  Al-Awadi/Raas-Rothschild syndrome
Reference
PMID:35052478
  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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