Unexplained kidney failure in young people
Gene: RENEnsemblGeneIds (GRCh38): ENSG00000143839
EnsemblGeneIds (GRCh37): ENSG00000143839
OMIM: 179820, Gene2Phenotype
REN is in 7 panels
1 review
Sarah Leigh (Genomics England Curator)
Comment when marking as ready: Associated with phenotype in OMIM, not in G2P. At least four variants reported in Renal tubular dysgenesis 267430, two in Hyperuricemic nephropathy, familial juvenile 2 613092 and one in HyperproreninemiaCreated: 5 Aug 2016, 9:36 a.m.
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- UKGTN
- Expert list
- Radboud University Medical Center, Nijmegen
- Illumina TruGenome Clinical Sequencing Services
- Phenotypes
-
- Hyperuricemic nephropathy, familial juvenile 2 613092
- Renal tubular dysgenesis 267430
- [Hyperproreninemia]
- OMIM
- 179820
- Clinvar variants
- Variants in REN
- 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).
Upload gene information
Sarah Leigh (Genomics England Curator)REN was added to Unexplained kidney failure in young peoplepanel. Sources: UKGTN
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for REN were set to Hyperuricemic nephropathy, familial juvenile 2 613092; Renal tubular dysgenesis 267430; [Hyperproreninemia]
Added New Source
Sarah Leigh (Genomics England Curator)REN was added to Unexplained kidney failure in young peoplepanel. Sources: Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,Expert list,Expert Review Green
Created
Sarah Leigh (Genomics England Curator)REN was created by sleigh