KEGG   VARIANT: 343637v1
Entry
343637v1                      Variant                              
Name
RSPO4 mutation
Type
Loss of function
Gene
RSPO4  R-spondin 4 [KO:K23099]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 610573
Network
nt06505  WNT signaling
Disease
H01307  Nonsyndromic congenital nail disorder
Reference
PMID:19619488
  Authors
MacDonald BT, Tamai K, He X
  Title
Wnt/beta-catenin signaling: components, mechanisms, and diseases.
  Journal
Dev Cell 17:9-26 (2009)
DOI:10.1016/j.devcel.2009.06.016
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