1. Panels
  2. Cerebellar and Pontocerebellar Hypoplasia
  3. FZD3
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Cerebellar and Pontocerebellar Hypoplasia

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

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find evidence for Mendelian gene-disease association. Some evidence for association of polymorphisms in this gene with schizophrenia, and some animal data supporting link with autism.
Created: 5 Jan 2020, 3:58 a.m. | Last Modified: 5 Jan 2020, 3:58 a.m.
Panel Version: 0.3
Created: 5 Jan 2020, 3:58 a.m.
Last Modified: 5 Jan 2020, 3:58 a.m.
Panel version: 0.3

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
606143
Clinvar variants
Variants in FZD3
Penetrance
None
Panels with this gene

History Filter Activity

5 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fzd3 has been classified as Red List (Low Evidence).

5 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fzd3 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: FZD3 was added gene: FZD3 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: FZD3 was set to Unknown