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Test MOI validation panel - do not edit

Gene: WNT5A

Green List (high evidence)
WNT5A (Wnt family member 5A)
EnsemblGeneIds (GRCh38): ENSG00000114251
EnsemblGeneIds (GRCh37): ENSG00000114251
OMIM: 164975, Gene2Phenotype
WNT5A is in 8 panels

0 reviews

Details

Mode of Inheritance
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Allowed values MOI test - gene on chr 3 but has an X-chromosome MOI
  • Across panels tests
OMIM
164975
Clinvar variants
Variants in WNT5A
Penetrance
None
Panels with this gene

History Filter Activity

20 Oct 2020, Gel status: 3

Set Phenotypes

Eleanor Williams (Genomics England Curator)

Phenotypes for gene: WNT5A were changed from Test - gene on chr 3 but has an X-chromosome MOI to Allowed values MOI test - gene on chr 3 but has an X-chromosome MOI; Across panels tests

19 Aug 2020, Gel status: 3

Entity classified by Genomics England curator

Eleanor Williams (Genomics England Curator)

Gene: wnt5a has been classified as Green List (High Evidence).

19 Aug 2020, Gel status: 1

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

Eleanor Williams (Genomics England Curator)

gene: WNT5A was added gene: WNT5A was added to TEST mode of inheritance validation panel. Sources: Literature Mode of inheritance for gene: WNT5A was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Phenotypes for gene: WNT5A were set to Test - gene on chr 3 but has an X-chromosome MOI