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  2. Hand and foot malformations
  3. WNT3
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Hand and foot malformations

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

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Single family reported.
Created: 3 Mar 2020, 11:42 p.m. | Last Modified: 3 Mar 2020, 11:42 p.m.
Panel Version: 0.1609

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Tetra-amelia syndrome 1, MIM# 273395

Publications

Created: 3 Mar 2020, 11:42 p.m.
Last Modified: 3 Mar 2020, 11:42 p.m.
Panel version: Imported from Mendeliome panel version 0.1609

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
  • Victorian Clinical Genetics Services
Phenotypes
  • Tetra-amelia syndrome 273395
OMIM
165330
Clinvar variants
Variants in WNT3
Penetrance
None
Publications
Panels with this gene

History Filter Activity

23 Sep 2021, Gel status: 1

Entity classified by Genomics England curator

Bryony Thompson (Royal Melbourne Hospital)

Gene: wnt3 has been classified as Red List (Low Evidence).

23 Sep 2021, Gel status: 1

Set publications

Bryony Thompson (Royal Melbourne Hospital)

Publications for gene: WNT3 were set to

22 Sep 2021, Gel status: 1

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

Bryony Thompson (Royal Melbourne Hospital)

gene: WNT3 was added gene: WNT3 was added to Hand and foot malformation. Sources: Expert list Mode of inheritance for gene: WNT3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: WNT3 were set to Tetra-amelia syndrome 273395