Lymphoedema_syndromic

Gene: ALX3

Red List (low evidence)

ALX3 (ALX homeobox 3)
EnsemblGeneIds (GRCh38): ENSG00000156150
EnsemblGeneIds (GRCh37): ENSG00000156150
OMIM: 606014, Gene2Phenotype
ALX3 is in 10 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • UKGTN
  • Radboud University Medical Center, Nijmegen
  • Expert Review Red
Phenotypes
  • Frontonasal dysplasia 1 136760
OMIM
606014
Clinvar variants
Variants in ALX3
Penetrance
None
Publications
Panels with this gene

History Filter Activity

29 Jan 2020, Gel status: 1

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

Sue White (Victorian Clinical Genetics Services)

gene: ALX3 was added gene: ALX3 was added to Lymphoedema_syndromic. Sources: Expert Review Red,Radboud University Medical Center, Nijmegen,UKGTN Mode of inheritance for gene: ALX3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ALX3 were set to 15127764 Phenotypes for gene: ALX3 were set to Frontonasal dysplasia 1 136760