Limb disordersGene: WNT10B
Comment when marking as ready: Associated with phenotype in OMIM and G2P. At least three variants reported
Created: 1 Aug 2016, 9:46 a.m.
Created: 17 Jun 2016, 8:09 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Split-hand/foot malformation 6 225300
Variants in this GENE are reported as part of current diagnostic practice
Phenotypes for gene: WNT10B were changed from Split-hand/foot malformation 6 225300 to Split-hand/foot malformation 6, OMIM:225300
Ana Beleza: Tier 2
Expert Review Green was added to WNT10B. Panel: Limb disorders Radboud University Medical Center, Nijmegen was added to WNT10B. Panel: Limb disorders Expert list was added to WNT10B. Panel: Limb disorders Model of inheritance for gene WNT10B was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene WNT10B was set to ['24211389']
London South East RGC GSTT was added to WNT10B. Panel: Limb disorders
WNT10B was added to Limb disorders panel. Sources: Viapath
WNT10B was created by Ellen McDonagh