Genomics England
GMS Panels
Panels
Genes and Entities

MEN1

menin 1
OMIM: 613733
PanelMode of inheritanceDetails
5 panels
Green
in Adult solid tumours cancer susceptibility
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Multiple Endocrine Neoplasia
Green
in Childhood solid tumours
R-numbers: R359
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Multiple Endocrine Neoplasia, Multiple endocrine neoplasia 1, 131100
Green
in Endocrine neoplasia
R-numbers: R217
Signed-off version 3.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Endocrine Cancer, pituitary tumours, Multiple Endocrine Neoplasia Type 1: MEN1 Gene Deletion/Duplication, Parathyroid adenoma, somatic, Multiple endocrine neoplasia 1, 131100, Carcinoid tumor of lung, Angiofibroma, somatic, Adrenal adenoma, somatic, Lipoma, somatic, MEN1-like spectrum, Multiple Endocrine Neoplasia
Green
in Familial hyperparathyroidism or hypocalciuric hypercalcaemia
R-numbers: R151
Signed-off version 3.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Multiple endocrine neoplasia 1 (131100), Familial isolated hyperparathyroidism
Green
in Inherited phaeochromocytoma and paraganglioma excluding NF1
R-numbers: R223
Signed-off version 2.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Multiple endocrine neoplasia type 1 (MEN1), Multiple Endocrine Neoplasia