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
- Fetal anomalies
- Inherited phaeochromocytoma and paraganglioma excluding NF1
- Unexplained kidney failure in young people
- Endocrine neoplasia
- Multiple endocrine tumours
- Thyroid cancer pertinent cancer susceptibility
- Gastrointestinal epithelial barrier disorders
- Childhood solid tumours cancer susceptibility
- Sudden death in young people
- Inherited phaeochromocytoma and paraganglioma
- Paediatric pseudo-obstruction syndrome
- CAKUT
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Additional findings health related - children
- Parathyroid Cancer
- COVID-19 research
- Familial Hirschsprung Disease
- Adult solid tumours for rare disease
- Unexplained young onset end-stage renal disease - additional genes
- Intellectual disability
- Childhood solid tumours
- Multiple endocrine neoplasia type 2
- Familial hyperparathyroidism or Hypocalciuric hypercalcaemia
- Additional findings health related
- Neuroendocrine cancer pertinent cancer susceptibility
- DDG2P
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