This Panel is marked as Deleted
Immunological disorders_SuperPanel_PanelAppAustralia
Gene: CARD14
CARD14 (caspase recruitment domain family member 14)
EnsemblGeneIds (GRCh38): ENSG00000141527
EnsemblGeneIds (GRCh37): ENSG00000141527
OMIM: 607211, Gene2Phenotype
CARD14 is in 11 panels
EnsemblGeneIds (GRCh38): ENSG00000141527
EnsemblGeneIds (GRCh37): ENSG00000141527
OMIM: 607211, Gene2Phenotype
CARD14 is in 11 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- Melbourne Genomics Health Alliance Immunology Flagship
- OMIM
- 607211
- Clinvar variants
- Variants in CARD14
- Penetrance
- None
- Panels with this gene
-
- Palmoplantar keratoderma and erythrokeratodermas
- Generalised pustular psoriasis
- Rare genetic inflammatory skin disorders
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Autoinflammatory disorders
- Epidermolysis bullosa and congenital skin fragility
- Ichthyosis and erythrokeratoderma
- COVID-19 research
- Peeling skin syndrome
- Pityriasis rubra pilaris
- Mosaic skin disorders - deep sequencing
History Filter Activity
7 Apr 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance
Rebecca Foulger (Genomics England curator)gene: CARD14 was added gene: CARD14 was added to Immunological disorders_SuperPanel_PanelAppAustralia. Sources: Melbourne Genomics Health Alliance Immunology Flagship,Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CARD14 was set to Unknown