This Panel is marked as Retired
NCGC
Gene: RET
RET (ret proto-oncogene)
EnsemblGeneIds (GRCh38): ENSG00000165731
EnsemblGeneIds (GRCh37): ENSG00000165731
OMIM: 164761, Gene2Phenotype
RET is in 23 panels
EnsemblGeneIds (GRCh38): ENSG00000165731
EnsemblGeneIds (GRCh37): ENSG00000165731
OMIM: 164761, Gene2Phenotype
RET is in 23 panels
0 reviews
Details
- Mode of Inheritance
- Other
- Sources
-
- NCGC
- Phenotypes
-
- Multiple endocrine neoplasia, type 2b
- Multiple endocrine neoplasia, type 2a
- Familial medullary thyroid carcinoma
- OMIM
- 164761
- Clinvar variants
- Variants in RET
- Penetrance
- None
- Panels with this gene
-
- Calcium and Phosphate disorders
- Incidentalome_PREGEN_DRAFT
- Gastrointestinal neuromuscular disease
- Parathyroid Tumour
- Hirschsprung disease
- BabyScreen+ newborn screening
- Vasculitis
- Intellectual disability syndromic and non-syndromic
- Transplant Co-Morbidity Superpanel
- Cancer Predisposition_Paediatric
- Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic
- Paraganglioma_phaeochromocytoma
- Facial papules
- Incidentalome
- Fetal anomalies
- Additional findings_Paediatric
- Additional findings_Adult
- Central Hypoventilation
- Cataract
- Renal Tubulopathies and related disorders
- Interstitial Lung Disease
- Hypercalcaemia
- Thyroid Cancer
History Filter Activity
7 Jan 2020, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Lavinia Gordon (UMCCR)gene: RET was added gene: RET was added to NCGC. Sources: NCGC Mode of inheritance for gene: RET was set to Other Phenotypes for gene: RET were set to Multiple endocrine neoplasia, type 2b; Multiple endocrine neoplasia, type 2a; Familial medullary thyroid carcinoma