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
- 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
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