Childhood solid tumours cancer susceptibility
Gene: NF2EnsemblGeneIds (GRCh38): ENSG00000186575
EnsemblGeneIds (GRCh37): ENSG00000186575
OMIM: 607379, Gene2Phenotype
NF2 is in 10 panels
1 review
Clare Turnbull (Queen Mary University London)
Tumour suppressor.Created: 5 Jul 2017, 11:28 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Acoustic neuroma
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Acoustic neuroma
- OMIM
- 607379
- Clinvar variants
- Variants in NF2
- Penetrance
- Complete
- Publications
- Panels with this gene
-
- Familial tumours of the nervous system
- Childhood solid tumours
- Familial Tumours Syndromes of the central & peripheral Nervous system
- Adult solid tumours cancer susceptibility
- Structural eye disease
- Mosaic skin disorders - deep sequencing
- Pigmentary skin disorders
- Bilateral congenital or childhood onset cataracts
- Childhood solid tumours cancer susceptibility
- Adult solid tumours for rare disease
History Filter Activity
Panel promoted to version 1.0
Louise Daugherty (Genomics England Curator)Clare Turnbull: Tumour suppressor.
Added New Source
Ellen McDonagh (Genomics England Curator)NF2 was added to Childhood solid tumourspanel. Source: Expert Review Green
Created
Ellen McDonagh (Genomics England Curator)NF2 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)NF2 was added to Childhood solid tumourspanel. Sources: Expert list