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Clefting disorders

Gene: WNT3

Red List (low evidence)

WNT3 (Wnt family member 3)
EnsemblGeneIds (GRCh38): ENSG00000108379
EnsemblGeneIds (GRCh37): ENSG00000108379
OMIM: 165330, Gene2Phenotype
WNT3 is in 8 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE
  • TETAMS
OMIM
165330
Clinvar variants
Variants in WNT3
Penetrance
None
Publications
Panels with this gene

History Filter Activity

16 Sep 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: WNT3 was added gene: WNT3 was added to Clefting_GEL. Sources: Expert Review Red Mode of inheritance for gene: WNT3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: WNT3 were set to 14872406 Phenotypes for gene: WNT3 were set to TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE; TETAMS