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Mendeliome

Gene: UGT1A4

Red List (low evidence)

UGT1A4 (UDP glucuronosyltransferase family 1 member A4)
EnsemblGeneIds (GRCh38): ENSG00000244474
EnsemblGeneIds (GRCh37): ENSG00000244474
OMIM: 606429, Gene2Phenotype
UGT1A4 is in 3 panels

2 reviews

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Comment when marking as ready: Agree, no evidence currently for Mendelian gene-disease association.
Created: 17 Feb 2020, 2:12 a.m. | Last Modified: 17 Feb 2020, 2:12 a.m.
Panel Version: 0.1374

Belinda Chong (Victorian Clinical Genetics Services)

Red List (low evidence)

No current disease association (? pharmacogenetics).
Created: 16 Feb 2020, 11:12 p.m. | Last Modified: 16 Feb 2020, 11:12 p.m.
Panel Version: 0.1373

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
606429
Clinvar variants
Variants in UGT1A4
Penetrance
None
Panels with this gene

History Filter Activity

17 Feb 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ugt1a4 has been classified as Red List (Low Evidence).

17 Feb 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ugt1a4 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: UGT1A4 was added gene: UGT1A4 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: UGT1A4 was set to Unknown