This Panel is marked as Deleted
Microcephaly Victorian Clinical Genetics Services
Gene: LIG4
LIG4 (DNA ligase 4)
EnsemblGeneIds (GRCh38): ENSG00000174405
EnsemblGeneIds (GRCh37): ENSG00000174405
OMIM: 601837, Gene2Phenotype
LIG4 is in 13 panels
EnsemblGeneIds (GRCh38): ENSG00000174405
EnsemblGeneIds (GRCh37): ENSG00000174405
OMIM: 601837, Gene2Phenotype
LIG4 is in 13 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 601837
- Clinvar variants
- Variants in LIG4
- Penetrance
- None
- Panels with this gene
-
- IUGR and IGF abnormalities
- Severe microcephaly
- COVID-19 research
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Intellectual disability
- DDG2P
- Monogenic short stature
- Gastrointestinal epithelial barrier disorders
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Haematological malignancies for rare disease
- Fetal anomalies
- Haematological malignancies cancer susceptibility
- Cytopenia - NOT Fanconi anaemia
History Filter Activity
21 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)LIG4 was added to Microcephaly Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
21 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)LIG4 was created by Sarah Leigh