Thyroid cancer pertinent cancer susceptibility
Gene: WRNEnsemblGeneIds (GRCh38): ENSG00000165392
EnsemblGeneIds (GRCh37): ENSG00000165392
OMIM: 604611, Gene2Phenotype
WRN is in 17 panels
1 review
Ellen McDonagh (Genomics England Curator)
This gene was reviewed by Lara Hawkes (Cancer Clinical Team, Genomics England) and there are no changes to make.Created: 20 Aug 2018, 1:31 p.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Werner syndrome
- Sarcoma
- Melanoma
- Thyroid cancer
- OMIM
- 604611
- Clinvar variants
- Variants in WRN
- Penetrance
- None
- Publications
- Panels with this gene
-
- Sarcoma cancer susceptibility
- Primary ovarian insufficiency
- Insulin resistance (including lipodystrophy)
- Intellectual disability
- Monogenic short stature
- Osteogenesis imperfecta
- Bilateral congenital or childhood onset cataracts
- Sarcoma susceptibility
- Childhood solid tumours
- Lipodystrophy - childhood onset
- IUGR and IGF abnormalities
- Structural eye disease
- Inherited non-medullary thyroid cancer
- Thyroid cancer pertinent cancer susceptibility
- Skeletal dysplasia
- Childhood solid tumours cancer susceptibility
- Monogenic diabetes
History Filter Activity
Panel promoted to version 1.0
Louise Daugherty (Genomics England Curator)Ellen McDonagh: This gene was reviewed by Lara
Entity classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)Gene: wrn has been classified as Green List (High Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)WRN was added to Thyroid cancer pertinent cancer susceptibility panel. Sources: Expert list
Created
Ellen McDonagh (Genomics England Curator)WRN was created by Ellen McDonagh