Disorders of immune dysregulation
Gene: IL10EnsemblGeneIds (GRCh38): ENSG00000136634
EnsemblGeneIds (GRCh37): ENSG00000136634
OMIM: 124092, Gene2Phenotype
IL10 is in 6 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
At least two families and a mouse model.
Rare variants in this gene are also associated with susceptibility to a range of immune-related complex disorders.Created: 17 Mar 2022, 8:39 p.m. | Last Modified: 17 Mar 2022, 8:41 p.m.
Panel Version: 0.11523
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Diseases of Immune Dysregulation; Early-onset inflammatory bowel disease
Publications
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Green
- Melbourne Genomics Health Alliance Immunology Flagship
- Victorian Clinical Genetics Services
- Expert Review Green
- Victorian Clinical Genetics Services
- OMIM
- 124092
- Clinvar variants
- Variants in IL10
- Penetrance
- None
- Panels with this gene
History Filter Activity
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: IL10 was added gene: IL10 was added to Disorders of immune dysregulation_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship Mode of inheritance for gene: IL10 was set to Unknown