This Panel is marked as Deleted
Immunological disorders_SuperPanel_PanelAppAustralia
Gene: IFIH1
IFIH1 (interferon induced with helicase C domain 1)
EnsemblGeneIds (GRCh38): ENSG00000115267
EnsemblGeneIds (GRCh37): ENSG00000115267
OMIM: 606951, Gene2Phenotype
IFIH1 is in 17 panels
EnsemblGeneIds (GRCh38): ENSG00000115267
EnsemblGeneIds (GRCh37): ENSG00000115267
OMIM: 606951, Gene2Phenotype
IFIH1 is in 17 panels
0 reviews
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic, autosomal or pseudoautosomal
- Sources
-
- Expert list
- Expert Review Green
- Phenotypes
-
- Rhinovirus and other RNA viruses
- Severe viral respiratory infections
- OMIM
- 606951
- Clinvar variants
- Variants in IFIH1
- Penetrance
- None
- Publications
- Panels with this gene
-
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Structural basal ganglia disorders
- Intellectual disability
- Intracerebral calcification disorders
- COVID-19 research
- Inherited white matter disorders
- Childhood onset dystonia, chorea or related movement disorder
- Structural eye disease
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Skeletal dysplasia
- Early onset or syndromic epilepsy
- Adult onset dystonia, chorea or related movement disorder
- Childhood onset hereditary spastic paraplegia
- Fetal anomalies
- DDG2P
- White matter disorders and cerebral calcification - narrow panel
- Glaucoma (developmental)
History Filter Activity
7 Apr 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: IFIH1 was added gene: IFIH1 was added to Immunological disorders_SuperPanel_PanelAppAustralia. Sources: Expert Review Green,Expert list Mode of inheritance for gene: IFIH1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: IFIH1 were set to 29018476; 28716935 Phenotypes for gene: IFIH1 were set to Rhinovirus and other RNA viruses; Severe viral respiratory infections