Transplant Co-Morbidity Superpanel
Gene: MEN1
MEN1 (menin 1)
EnsemblGeneIds (GRCh38): ENSG00000133895
EnsemblGeneIds (GRCh37): ENSG00000133895
OMIM: 613733, Gene2Phenotype
MEN1 is in 15 panels
EnsemblGeneIds (GRCh38): ENSG00000133895
EnsemblGeneIds (GRCh37): ENSG00000133895
OMIM: 613733, Gene2Phenotype
MEN1 is in 15 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Melbourne Genomics Health Alliance
- Phenotypes
-
- Multiple endocrine neoplasia 1, MIM# 131100
- OMIM
- 613733
- Clinvar variants
- Variants in MEN1
- Penetrance
- None
- Panels with this gene
-
- Calcium and Phosphate disorders
- Hyperinsulinism
- Incidentalome_PREGEN_DRAFT
- Pituitary Tumour
- Parathyroid Tumour
- BabyScreen+ newborn screening
- Transplant Co-Morbidity Superpanel
- Cancer Predisposition_Paediatric
- Paraganglioma_phaeochromocytoma
- Facial papules
- Incidentalome
- Additional findings_Paediatric
- Additional findings_Adult
- Renal Tubulopathies and related disorders
- Hypercalcaemia
History Filter Activity
1 Aug 2023, Gel status: 3
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: MEN1 was added gene: MEN1 was added to Transplant Co-Morbidity Superpanel. Sources: Melbourne Genomics Health Alliance,Expert Review Green Mode of inheritance for gene: MEN1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: MEN1 were set to Multiple endocrine neoplasia 1, MIM# 131100