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