1. Panels
  2. Familial tumours of the nervous system
  3. NF2
STRs in panel
Prev Next
Regions in panel
Prev Next

Familial tumours of the nervous system

Gene: NF2

Green List (high evidence)
NF2 (neurofibromin 2)
EnsemblGeneIds (GRCh38): ENSG00000186575
EnsemblGeneIds (GRCh37): ENSG00000186575
OMIM: 607379, Gene2Phenotype
NF2 is in 10 panels

1 review

Achchuthan Shanmugasundram (Genomics England Curator)

Green List (high evidence)

Comment on phenotypes: This gene has been associated with MIM #101000 in OMIM and the OMIM record was last accessed on 29 December 2025.
Created: 29 Dec 2025, 2:48 p.m. | Last Modified: 29 Dec 2025, 2:48 p.m.
Panel Version: 2.10
NF2 has been added to the panel for R221 Familial tumours of the nervous system with a green rating as agreed with the NHS Genomic Medicine Service.
Created: 30 Jun 2023, 1:12 p.m. | Last Modified: 30 Jun 2023, 1:12 p.m.
Panel Version: 0.1

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Created: 30 Jun 2023, 1:12 p.m.
Last Modified: 30 Jun 2023, 1:12 p.m.
Panel version: 0.1

History Filter Activity

29 Dec 2025, Gel status: 3

Set Phenotypes

Achchuthan Shanmugasundram (Genomics England Curator)

Phenotypes for gene: NF2 were changed from to Schwannomatosis, vestibular, OMIM:101000; NF2-related schwannomatosis, MONDO:0007039

29 Jun 2023, Gel status: 3

Created, Added New Source, Set mode of inheritance

Achchuthan Shanmugasundram (Genomics England Curator)

gene: NF2 was added gene: NF2 was added to Familial tumours of the nervous system. Sources: NHS GMS,Expert Review Green Mode of inheritance for gene: NF2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown