1. Panels
  2. Test panel testing 2020-07-27
  3. ALX4

Test panel testing 2020-07-27

Gene: ALX4

Green List (high evidence)
ALX4 (ALX homeobox 4)
EnsemblGeneIds (GRCh38): ENSG00000052850
EnsemblGeneIds (GRCh37): ENSG00000052850
OMIM: 605420, Gene2Phenotype
ALX4 is in 5 panels

1 review

Eleanor Williams (Genomics England Curator)

I don't know

Test of Amber review
Created: 27 Jul 2020, 12:09 p.m. | Last Modified: 27 Jul 2020, 12:09 p.m.
Panel Version: 1.6

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

Phenotypes
Phentoype 2

Publications

Created: 27 Jul 2020, 12:09 p.m.
Last Modified: 27 Jul 2020, 12:09 p.m.
Panel version: 1.6

Details

Mode of Inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Parietal foramina 2, (AD), 609597
  • Frontonasal dysplasia 2, (AR), 613451
  • Parietal foramina
Tags
watchlist
OMIM
605420
Clinvar variants
Variants in ALX4
Penetrance
None
Publications
Panels with this gene

History Filter Activity

27 Jul 2020, Gel status: 3

Added Tag

Sarah Leigh (Genomics England Curator)

Tag watchlist tag was added to gene: ALX4.

27 Jul 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Eleanor Williams (Genomics England Curator)

gene: ALX4 was added gene: ALX4 was added to Test panel testing 2020-07-27. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: ALX4 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: ALX4 were set to 29215649; 22829454; 29681084 Phenotypes for gene: ALX4 were set to Parietal foramina 2, (AD), 609597; Frontonasal dysplasia 2, (AR), 613451; Parietal foramina