Palmoplantar keratodermas
Gene: KRT2EnsemblGeneIds (GRCh38): ENSG00000172867
EnsemblGeneIds (GRCh37): ENSG00000172867
OMIM: 600194, Gene2Phenotype
KRT2 is in 4 panels
1 review
Rebecca Foulger (Genomics England curator)
This gene was part of an initial gene list collated by Thomas Cullup, GOSH and Veronica Kinsler, UCL, 25.Jan.2019 on behalf of the GMS Skin Specialist Test Group. Gene Symbol submitted: KRT2; 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: 28 Jan 2019, 10:47 a.m.
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- London North GLH
- NHS GMS
- Expert Review Green
- Phenotypes
-
- Autosomal dominant ichthyosis
- OMIM
- 600194
- Clinvar variants
- Variants in KRT2
- Penetrance
- None
- Panels with this gene
History Filter Activity
Added New Source
Rebecca Foulger (Genomics England curator)Source London North GLH was added to KRT2.
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: KRT2 was added gene: KRT2 was added to Palmoplantar keratodermas. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: KRT2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: KRT2 were set to Autosomal dominant ichthyosis