Multiple endocrine tumours
Gene: MEN1EnsemblGeneIds (GRCh38): ENSG00000133895
EnsemblGeneIds (GRCh37): ENSG00000133895
OMIM: 613733, Gene2Phenotype
MEN1 is in 16 panels
4 reviews
Louise IZATT (GSTT Clinical Genetics Service)
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Katie Snape (South London GMC)
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Variants in this GENE are reported as part of current diagnostic practice
Treena Cranston (Oxford)
Sian Ellard (University of Exeter Medical School)
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Eligibility statement prior genetic testing
- Expert
- Radboud University Medical Center, Nijmegen
- Illumina TruGenome Clinical Sequencing Services
- UKGTN
- Emory Genetics Laboratory
- Phenotypes
-
- 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
- OMIM
- 613733
- Clinvar variants
- Variants in MEN1
- Penetrance
- Complete
- Panels with this gene
-
- Inherited phaeochromocytoma and paraganglioma
- Additional findings health related - children
- Familial Tumours Syndromes of the central & peripheral Nervous system
- Parathyroid Cancer
- Familial hyperparathyroidism or hypocalciuric hypercalcaemia
- Adult solid tumours for rare disease
- Childhood solid tumours
- Adult solid tumours cancer susceptibility
- Multiple endocrine tumours
- Endocrine neoplasia
- Additional findings health related - CNV analysis children
- Inherited phaeochromocytoma and paraganglioma excluding NF1
- Inherited non-medullary thyroid cancer
- Additional findings health related
- Neuroendocrine cancer pertinent cancer susceptibility
- Childhood solid tumours cancer susceptibility
History Filter Activity
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Set Phenotypes
Ellen McDonagh (Genomics England Curator)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
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Mode of inheritance for MEN1 was changed to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Set Phenotypes
Eik Haraldsdottir (Genomics England)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
Added New Source
Ellen McDonagh (Genomics England Curator)MEN1 was added to Multiple endocrine tumourspanel. Sources: Eligibility statement prior genetic testing
Added New Source
Eik Haraldsdottir (Genomics England)MEN1 was added to Multiple endocrine tumourspanel. Sources: Expert
Added New Source
GEL ()MEN1 was added to Multiple endocrine tumourspanel. Sources: Radboud University Medical Center, Nijmegen
Added New Source
GEL ()MEN1 was added to Multiple endocrine tumourspanel. Sources: Illumina TruGenome Clinical Sequencing Services
Added New Source
GEL ()MEN1 was added to Multiple endocrine tumourspanel. Sources: UKGTN
Added New Source
GEL ()MEN1 was added to Multiple endocrine tumourspanel. Sources: Emory Genetics Laboratory