Parathyroid Cancer
Gene: RETEnsemblGeneIds (GRCh38): ENSG00000165731
EnsemblGeneIds (GRCh37): ENSG00000165731
OMIM: 164761, Gene2Phenotype
RET is in 29 panels
1 review
Ellen Thomas (Genomics England Curator)
Comment when marking as ready: Parathyroid cancer not part of MEN2Created: 28 Feb 2016, 4:14 p.m.
Details
- Sources
-
- Expert Review Red
- UKGTN
- Phenotypes
-
- Pituitary Cancer, Parathyroid and Hypercalcemia
- 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
Gene classified by Genomics England curator
Ellen Thomas (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)RET was added to Parathyroid Cancerpanel. Sources: UKGTN