This Panel is marked as Deleted
Immunological disorders Victorian Clinical Genetics Services
Gene: IKBKG
IKBKG (inhibitor of nuclear factor kappa B kinase subunit gamma)
EnsemblGeneIds (GRCh38): ENSG00000269335
EnsemblGeneIds (GRCh37): ENSG00000073009
OMIM: 300248, Gene2Phenotype
IKBKG is in 19 panels
EnsemblGeneIds (GRCh38): ENSG00000269335
EnsemblGeneIds (GRCh37): ENSG00000073009
OMIM: 300248, Gene2Phenotype
IKBKG is in 19 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 300248
- Clinvar variants
- Variants in IKBKG
- Penetrance
- None
- Panels with this gene
-
- DDG2P
- COVID-19 research
- Ectodermal dysplasia
- Epidermolysis bullosa and congenital skin fragility
- Autoinflammatory disorders
- Fetal anomalies
- Mosaic skin disorders - deep sequencing
- Early onset or syndromic epilepsy
- Retinal disorders
- Ectodermal dysplasia without a known gene mutation
- Skeletal dysplasia
- Rare genetic inflammatory skin disorders
- Intellectual disability
- Incontinentia pigmenti
- Gastrointestinal epithelial barrier disorders
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Structural eye disease
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Primary lymphoedema
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)IKBKG was added to Immunological disorders Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)IKBKG was created by Sarah Leigh