Meningioma
Gene: NF2EnsemblGeneIds (GRCh38): ENSG00000186575
EnsemblGeneIds (GRCh37): ENSG00000186575
OMIM: 607379, Gene2Phenotype
NF2 is in 11 panels
1 review
Chirag Patel (Genetic Health Queensland)
ClinGen definitive. Meningiomas reported in condition.
Sources: Expert list, Expert ReviewCreated: 12 Sep 2024, 12:59 a.m. | Last Modified: 12 Sep 2024, 2:57 a.m.
Panel Version: 0.10
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Meningioma, MONDO:0016642; Neurofibromatosis type 2, MONDO:0007039; Neurofibromatosis, type 2, MIM#607174
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Expert Review
- Expert list
- Phenotypes
-
- Meningioma, MONDO:0016642
- Neurofibromatosis type 2, MONDO:0007039
- Neurofibromatosis, type 2, MIM#607174
- OMIM
- 607379
- Clinvar variants
- Variants in NF2
- Penetrance
- None
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: nf2 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Chirag Patel (Genetic Health Queensland)Gene: nf2 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Chirag Patel (Genetic Health Queensland)gene: NF2 was added gene: NF2 was added to Meningioma. Sources: Expert list,Expert Review Mode of inheritance for gene: NF2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: NF2 were set to Meningioma, MONDO:0016642; Neurofibromatosis type 2, MONDO:0007039; Neurofibromatosis, type 2, MIM#607174 Review for gene: NF2 was set to GREEN gene: NF2 was marked as current diagnostic