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Callosome

Gene: ALX3

Green List (high evidence)

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

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Intellectual disability is part of the phenotype.
Created: 23 Nov 2019, 7:20 a.m. | Last Modified: 23 Nov 2019, 7:20 a.m.
Panel Version: 0.1

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Frontonasal dysplasia 1, MIM#136760

Publications

Details

Mode of Inheritance
Unknown
Sources
  • Genetic Health Queensland
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • Expert Review Green
OMIM
606014
Clinvar variants
Variants in ALX3
Penetrance
None
Panels with this gene

History Filter Activity

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: ALX3 was added gene: ALX3 was added to Corpus callosum agenesis, Callosome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ALX3 was set to Unknown