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  3. ALX3
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Pierre Robin Sequence

Gene: ALX3

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

1 review

Tiong Tan (Victorian Clinical Genetics Services)

I don't know

Frontorhiny; two sibs from same family with cleft palate, an unrelated individual with cleft lip. Insufficient evidence for cleft, and PRS criteria not formally fulfilled.
Created: 10 Feb 2021, 3:56 a.m. | Last Modified: 10 Feb 2021, 3:56 a.m.
Panel Version: 0.16

Phenotypes
frontorhiny

Created: 10 Feb 2021, 3:56 a.m.
Last Modified: 10 Feb 2021, 3:56 a.m.
Panel version: 0.16

History Filter Activity

10 Feb 2021, Gel status: 2

Entity classified by Genomics England curator

Tiong Tan (Victorian Clinical Genetics Services)

Gene: alx3 has been classified as Amber List (Moderate Evidence).

10 Feb 2021, Gel status: 2

Entity classified by Genomics England curator

Tiong Tan (Victorian Clinical Genetics Services)

Gene: alx3 has been classified as Amber List (Moderate Evidence).

10 Feb 2021, Gel status: 3

Entity classified by Genomics England curator

Tiong Tan (Victorian Clinical Genetics Services)

Gene: alx3 has been classified as Green List (High Evidence).

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 Pierre Robin sequence _VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ALX3 was set to Unknown