Multiple endocrine tumours
Gene: RET
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Variants in this GENE are reported as part of current diagnostic practice
Variants in this gene are already reported as part of UKGTN diagnostic service, but GeL will offer WGS analysis.Created: 16 Oct 2015, 12:53 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
This gene has been classified as Green List (High Evidence).
Mode of inheritance for RET was changed to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene RET were set to Multiple endocrine neoplasia IIA, 171400;Multiple Endocrine Neoplasia;Multiple Endocrine Neoplasia Type 2: RET Gene Deletion/Duplication;MEN2-like spectrum; Endocrine Cancer
RET was added to Multiple endocrine tumourspanel. Sources: Eligibility statement prior genetic testing
RET was added to Multiple endocrine tumourspanel. Sources: Eligibility Statements for GeL,Expert list
RET was added to Multiple endocrine tumourspanel. Sources: Eligibility Statements for GeL,Expert list
RET was added to Multiple endocrine tumourspanel. Sources: Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
RET was added to Multiple endocrine tumourspanel. Sources: Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
RET was added to Multiple endocrine tumourspanel. Sources: Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
RET was added to Multiple endocrine tumourspanel. Sources: Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN