Ichthyosis and erythrokeratoderma
Gene: PIGLEnsemblGeneIds (GRCh38): ENSG00000108474
EnsemblGeneIds (GRCh37): ENSG00000108474
OMIM: 605947, Gene2Phenotype
PIGL is in 11 panels
1 review
Catherine Snow (Genomics England)
Comment on list classification: Sufficient cases identified in OMIMCreated: 12 Dec 2019, 2:57 p.m. | Last Modified: 12 Dec 2019, 2:57 p.m.
Panel Version: 0.16
This gene was part of a gene list collated by John McGrath, KCL and Veronica Kinsler, UCL, 17.Jun.2019 on behalf of the GMS Skin Specialist Test Group. Gene Symbol submitted:PIGL; Suggested initial gene rating: Green; Evidence for inclusion: none provided; Evidence for exclusion: none provided; Technical notes (e.g. non-coding/CNV mutations requiring coverage?): none provided.Created: 9 Sep 2019, 3:38 p.m. | Last Modified: 9 Sep 2019, 3:38 p.m.
Panel Version: 0.10
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Phenotypes
-
- CHIME syndrome, OMIM:280000
- OMIM
- 605947
- Clinvar variants
- Variants in PIGL
- Penetrance
- None
- Panels with this gene
History Filter Activity
Set Phenotypes
Ivone Leong (Genomics England Curator)Phenotypes for gene: PIGL were changed from to CHIME syndrome, OMIM:280000
Entity classified by Genomics England curator
Catherine Snow (Genomics England)Gene: pigl has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance
Catherine Snow (Genomics England)gene: PIGL was added gene: PIGL was added to Ichthyosis and erythrokeratoderma. Sources: Expert Review Amber Mode of inheritance for gene: PIGL was set to BIALLELIC, autosomal or pseudoautosomal