Multiple endocrine tumours
Gene: MEN1
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Variants in this GENE are reported as part of current diagnostic practice
This gene has been classified as Green List (High Evidence).
Phenotypes for MEN1 were set to Multiple Endocrine Neoplasia Type 1: MEN1 Gene Deletion/Duplication; Multiple Endocrine Neoplasia; Multiple endocrine neoplasia 1, 131100; Carcinoid tumor of lung; Parathyroid adenoma, somatic; Lipoma, somatic; Angiofibroma, somatic; Adrenal adenoma, somatic; MEN1-like spectrum; pituitary tumours; Endocrine Cancer
Mode of inheritance for MEN1 was changed to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene MEN1 were set to Multiple Endocrine Neoplasia Type 1: MEN1 Gene Deletion/Duplication;Multiple Endocrine Neoplasia;Multiple endocrine neoplasia 1, 131100Carcinoid tumor of lung Parathyroid adenoma, somatic Lipoma, somatic Angiofibroma, somatic Adrenal adenoma, somatic;MEN1-like spectrum; pituitary tumours; Endocrine Cancer
MEN1 was added to Multiple endocrine tumourspanel. Sources: Eligibility statement prior genetic testing
MEN1 was added to Multiple endocrine tumourspanel. Sources: Expert
MEN1 was added to Multiple endocrine tumourspanel. Sources: Radboud University Medical Center, Nijmegen
MEN1 was added to Multiple endocrine tumourspanel. Sources: Illumina TruGenome Clinical Sequencing Services
MEN1 was added to Multiple endocrine tumourspanel. Sources: UKGTN
MEN1 was added to Multiple endocrine tumourspanel. Sources: Emory Genetics Laboratory