Ectodermal dysplasia

Gene: WNT7A

Red List (low evidence)

WNT7A (Wnt family member 7A)
EnsemblGeneIds (GRCh38): ENSG00000154764
EnsemblGeneIds (GRCh37): ENSG00000154764
OMIM: 601570, Gene2Phenotype
WNT7A is in 9 panels

1 review

Catherine Snow (Genomics England)

I don't know

Comment on list classification: Currently no gene disease association can be found.
Created: 2 Dec 2019, 3:58 p.m. | Last Modified: 2 Dec 2019, 3:58 p.m.
Panel Version: 0.24
This gene was part of a gene list collated by John McGrath, KCL and Veronica Kinsler, UCL, 17.Jun.2019 on behalf of the GMS Skin Specialist Test Group. Gene Symbol submitted: WNT7A; Suggested initial gene rating: Green; Evidence for inclusion: none provided; Evidence for exclusion: none provided; Technical notes (e.g. non-coding/CNV mutations requiring coverage?): none provided.
Created: 3 Sep 2019, 4:14 p.m. | Last Modified: 3 Sep 2019, 4:14 p.m.
Panel Version: 0.16


Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
  • Expert Review Red
  • Fuhrmann syndrome, 228930
Clinvar variants
Variants in WNT7A
Panels with this gene

History Filter Activity

2 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Catherine Snow (Genomics England)

Gene: wnt7a has been classified as Red List (Low Evidence).

3 Sep 2019, Gel status: 2

Set Phenotypes

Catherine Snow (Genomics England)

Phenotypes for gene: WNT7A were changed from to Fuhrmann syndrome, 228930

2 Sep 2019, Gel status: 2

Created, Added New Source, Set mode of inheritance

Catherine Snow (Genomics England)

gene: WNT7A was added gene: WNT7A was added to Ectodermal dysplasia. Sources: Expert Review Amber Mode of inheritance for gene: WNT7A was set to BIALLELIC, autosomal or pseudoautosomal