Multiple Tumours
Gene: ALKEnsemblGeneIds (GRCh38): ENSG00000171094
EnsemblGeneIds (GRCh37): ENSG00000171094
OMIM: 105590, Gene2Phenotype
ALK is in 4 panels
1 review
Ellen McDonagh (Genomics England Curator)
Information from TruSight panel: Pathogenic Mutations are Activating.Created: 5 Feb 2016, 11:46 a.m.
Mode of pathogenicity
Other - please provide details in the comments
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- TruSight Cancer Panel (Illumina)
- Phenotypes
-
- Neuroblastoma
- Paediatric congenital malformation-dysmorphism-tumour syndromes
- OMIM
- 105590
- Clinvar variants
- Variants in ALK
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Set Mode of Inheritance, Added New Source
Ellen McDonagh (Genomics England Curator)ALK was added to Multiple Tumourspanel. Source: Expert Review Green Model of inheritance for gene ALK was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Created
Ellen McDonagh (Genomics England Curator)ALK was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)ALK was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)