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Fetal anomalies

Gene: FZD6

Amber List (moderate evidence)

FZD6 (frizzled class receptor 6)
EnsemblGeneIds (GRCh38): ENSG00000164930
EnsemblGeneIds (GRCh37): ENSG00000164930
OMIM: 603409, Gene2Phenotype
FZD6 is in 3 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

I don't know

Three FZD6 variants have been associated with two unrelated cases of fetal hyrdrops.
Sources: Expert list
Created: 2 Aug 2024, 7:11 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Hydrops fetalis, MONDO:0015193, FZD6-related

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Hydrops fetalis, MONDO:0015193, FZD6-related
OMIM
603409
Clinvar variants
Variants in FZD6
Penetrance
None
Publications
Panels with this gene

History Filter Activity

2 Aug 2024, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fzd6 has been classified as Amber List (Moderate Evidence).

2 Aug 2024, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fzd6 has been classified as Amber List (Moderate Evidence).

2 Aug 2024, Gel status: 1

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: FZD6 was added gene: FZD6 was added to Fetal anomalies. Sources: Expert list Mode of inheritance for gene: FZD6 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FZD6 were set to 33082562; 26036949; 28425981 Phenotypes for gene: FZD6 were set to Hydrops fetalis, MONDO:0015193, FZD6-related Review for gene: FZD6 was set to AMBER