Sudden death in young people
Gene: RETEnsemblGeneIds (GRCh38): ENSG00000165731
EnsemblGeneIds (GRCh37): ENSG00000165731
OMIM: 164761, Gene2Phenotype
RET is in 29 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Other
- Phenotypes
-
- Central hypoventilation syndrome, congenital, 209880
- CCHS
- OMIM
- 164761
- Clinvar variants
- Variants in RET
- Penetrance
- Complete
- Panels with this gene
-
- Adult solid tumours cancer susceptibility
- Familial pulmonary fibrosis
- Gastrointestinal neuromuscular disorders
- Paediatric pseudo-obstruction syndrome
- Unexplained kidney failure in young people
- Multiple endocrine tumours
- Intellectual disability
- Thyroid cancer pertinent cancer susceptibility
- Gastrointestinal epithelial barrier disorders
- Familial hyperparathyroidism or hypocalciuric hypercalcaemia
- Unexplained young onset end-stage renal disease - additional genes
- Childhood solid tumours cancer susceptibility
- Sudden death in young people
- Inherited phaeochromocytoma and paraganglioma excluding NF1
- Inherited phaeochromocytoma and paraganglioma
- CAKUT
- Fetal anomalies
- Additional findings health related - children
- Endocrine neoplasia
- Parathyroid Cancer
- COVID-19 research
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Familial Hirschsprung Disease
- Adult solid tumours for rare disease
- DDG2P
- Childhood solid tumours
- Multiple endocrine neoplasia type 2
- Additional findings health related
- Neuroendocrine cancer pertinent cancer susceptibility
History Filter Activity
panel promoted to version 1
Ellen Thomas (Genomics England Curator)This panel contains genes which aren't arrhythmic or metabolic causes of sudden death with normal post mortem.
Created
Rebecca Foulger (Genomics England curator)RET was created by rfoulger
Added New Source
Rebecca Foulger (Genomics England curator)RET was added to Sudden death in young peoplepanel. Sources: Other