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Intellectual disability syndromic and non-syndromic

Gene: PON3

Red List (low evidence)

PON3 (paraoxonase 3)
EnsemblGeneIds (GRCh38): ENSG00000105852
EnsemblGeneIds (GRCh37): ENSG00000105852
OMIM: 602720, Gene2Phenotype
PON3 is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find evidence for gene-disease association.
Created: 8 Dec 2019, 11:36 p.m. | Last Modified: 8 Dec 2019, 11:36 p.m.
Panel Version: 0.983

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Genetic Health Queensland
OMIM
602720
Clinvar variants
Variants in PON3
Penetrance
None
Panels with this gene

History Filter Activity

8 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: pon3 has been classified as Red List (Low Evidence).

8 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: pon3 has been classified as Red List (Low Evidence).

22 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: PON3 was added gene: PON3 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland Mode of inheritance for gene: PON3 was set to Unknown