Intracerebral calcification disorders
Gene: USP18EnsemblGeneIds (GRCh38): ENSG00000184979
EnsemblGeneIds (GRCh37): ENSG00000184979
OMIM: 607057, Gene2Phenotype
USP18 is in 9 panels
1 review
Ellen Thomas (Genomics England Curator)
Comment on list classification: One publication (recent), two families, segregation in 5 affected individuals plus an unaffected sibling, evidence of knock-out at protein level in the affected individuals.Created: 19 Dec 2016, 5:28 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
pseudo-TORCH syndrome
Publications
- PMID: 27325888
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- pseudo-TORCH syndrome
- OMIM
- 607057
- Clinvar variants
- Variants in USP18
- Penetrance
- Complete
- Publications
-
- PMID: 27325888
- Panels with this gene
-
- White matter disorders and cerebral calcification - narrow panel
- Cytopenias and congenital anaemias
- Intracerebral calcification disorders
- Intellectual disability
- Early onset or syndromic epilepsy
- COVID-19 research
- Primary immunodeficiency or monogenic inflammatory bowel disease
- DDG2P
- Fetal anomalies
History Filter Activity
panel promoted to version 1
Ellen McDonagh (Genomics England Curator)19th Dec 2016: panel revised according to expert review and internal curation review.
Gene classified by Genomics England curator
Ellen Thomas (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Gene classified by Genomics England curator
Ellen Thomas (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Ellen Thomas (Genomics England Curator)USP18 was added to Intracerebral calcification disorderspanel. Sources: Literature
Created
Ellen Thomas (Genomics England Curator)USP18 was created by EllenThomas