KEGG   VARIANT: 55366v1
Entry
55366v1                      Variant                               
Name
LGR4 mutation
Type
Loss of function
Gene
LGR4  leucine rich repeat containing G protein-coupled receptor 4 [KO:K04309]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 606666
Network
nt06505  WNT signaling
Disease
H01593  Osteoporosis
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
Reference
  Authors
Doherty L, Sanjay A
  Title
LGRs in Skeletal Tissues: An Emerging Role for Wnt-Associated Adult Stem Cell Markers in Bone.
  Journal
JBMR Plus 4:e10380 (2020)
DOI:10.1002/jbm4.10380
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