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Hearing loss

Gene: FZD3

Red List (low evidence)

FZD3 (frizzled class receptor 3)
EnsemblGeneIds (GRCh38): ENSG00000104290
EnsemblGeneIds (GRCh37): ENSG00000104290
OMIM: 606143, Gene2Phenotype
FZD3 is in 3 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

FZD3 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:06 a.m.
FZD3 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:42 p.m.

Publications

Details

Sources
  • Expert
OMIM
606143
Clinvar variants
Variants in FZD3
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

FZD3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert