This Panel is marked as Deleted
Test panel testing 2020-07-27
Gene: ALX3
ALX3 (ALX homeobox 3)
EnsemblGeneIds (GRCh38): ENSG00000156150
EnsemblGeneIds (GRCh37): ENSG00000156150
OMIM: 606014, Gene2Phenotype
ALX3 is in 9 panels
EnsemblGeneIds (GRCh38): ENSG00000156150
EnsemblGeneIds (GRCh37): ENSG00000156150
OMIM: 606014, Gene2Phenotype
ALX3 is in 9 panels
1 review
Eleanor Williams (Genomics England Curator)
Test of no colour rating in reviewCreated: 27 Jul 2020, 12:09 p.m. | Last Modified: 27 Jul 2020, 12:09 p.m.
Panel Version: 1.6
Details
- Sources
-
- NHS GMS
- Expert Review Red
- Phenotypes
-
- Frontonasal dysplasia type 1 (frontorhiny)
- OMIM
- 606014
- Clinvar variants
- Variants in ALX3
- Penetrance
- None
- Panels with this gene
History Filter Activity
27 Jul 2020, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Eleanor Williams (Genomics England Curator)gene: ALX3 was added gene: ALX3 was added to Test panel testing 2020-07-27. Sources: Expert Review Red,NHS GMS Mode of inheritance for gene: ALX3 was set to Phenotypes for gene: ALX3 were set to Frontonasal dysplasia type 1 (frontorhiny)