Genes in panel

TEST Undiagnosed metabolic disorders

Gene: ABCG2

Red List (low evidence)

ABCG2 (ATP binding cassette subfamily G member 2 (Junior blood group))
EnsemblGeneIds (GRCh38): ENSG00000118777
EnsemblGeneIds (GRCh37): ENSG00000118777
OMIM: 603756, Gene2Phenotype
ABCG2 is in 3 panels

0 reviews

Details

Mode of Inheritance
Unknown
Sources
  • Literature
  • Expert Review Red
OMIM
603756
Clinvar variants
Variants in ABCG2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Aug 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications

Sarah Leigh (Genomics England Curator)

gene: ABCG2 was added gene: ABCG2 was added to TEST Undiagnosed metabolic disorders. Sources: Expert Review Red,Literature Mode of inheritance for gene: ABCG2 was set to Unknown Publications for gene: ABCG2 were set to 27604308