Genes in panel
Regions in panel
Prev Next

Mendeliome

Gene: GSTO2

Red List (low evidence)

GSTO2 (glutathione S-transferase omega 2)
EnsemblGeneIds (GRCh38): ENSG00000065621
EnsemblGeneIds (GRCh37): ENSG00000065621
OMIM: 612314, Gene2Phenotype
GSTO2 is in 1 panel

1 review

Bryony Thompson (Royal Melbourne Hospital)

Red List (low evidence)

Cannot find any reports in Mendelian disease, only reports of risk loci association studies.
Created: 4 Feb 2021, 11:14 p.m. | Last Modified: 4 Feb 2021, 11:14 p.m.
Panel Version: 0.6215

Mode of inheritance
Unknown

Publications

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
612314
Clinvar variants
Variants in GSTO2
Penetrance
None
Panels with this gene

History Filter Activity

4 Feb 2021, Gel status: 1

Entity classified by Genomics England curator

Bryony Thompson (Royal Melbourne Hospital)

Gene: gsto2 has been classified as Red List (Low Evidence).

4 Feb 2021, Gel status: 1

Entity classified by Genomics England curator

Bryony Thompson (Royal Melbourne Hospital)

Gene: gsto2 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: GSTO2 was added gene: GSTO2 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: GSTO2 was set to Unknown