Unexplained kidney failure in young people
Gene: AGTEnsemblGeneIds (GRCh38): ENSG00000135744
EnsemblGeneIds (GRCh37): ENSG00000135744
OMIM: 106150, Gene2Phenotype
AGT is in 8 panels
1 review
Sarah Leigh (Genomics England Curator)
Comment when marking as ready: Associated with phenotype in OMIM, not in G2P. At least three variants reportedCreated: 4 Aug 2016, 10:05 a.m.
Comment on phenotypes: Also associated with {Hypertension, essential, susceptibility to} 145500;{Preeclampsia, susceptibility to}Created: 4 Aug 2016, 10:05 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- UKGTN
- Radboud University Medical Center, Nijmegen
- Illumina TruGenome Clinical Sequencing Services
- Phenotypes
-
- Renal tubular dysgenesis, 267430
- OMIM
- 106150
- Clinvar variants
- Variants in AGT
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
panel promoted to version 1
Sarah Leigh (Genomics England Curator)Promoted to version 1 17th August 2016
Gene classified by Genomics England curator
Sarah Leigh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for AGT were set to Renal tubular dysgenesis, 267430
Upload gene information
Sarah Leigh (Genomics England Curator)AGT was added to Unexplained kidney failure in young peoplepanel. Sources: UKGTN
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for AGT were set to Renal tubular dysgenesis, 267430
Added New Source
Sarah Leigh (Genomics England Curator)AGT was added to Unexplained kidney failure in young peoplepanel. Sources: Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,Expert Review Green
Created
Sarah Leigh (Genomics England Curator)AGT was created by sleigh