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Mendeliome

Gene: XG

Red List (low evidence)

XG (Xg blood group)
EnsemblGeneIds (GRCh38): ENSG00000124343
EnsemblGeneIds (GRCh37): ENSG00000124343
OMIM: 300879, Gene2Phenotype
XG is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence for association with Mendelian disease.
Created: 3 Mar 2022, 7:36 a.m. | Last Modified: 3 Mar 2022, 7:36 a.m.
Panel Version: 0.11120

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
300879
Clinvar variants
Variants in XG
Penetrance
None
Panels with this gene

History Filter Activity

3 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

3 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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