Immunological disorders_SuperPanel_PanelAppAustralia
Gene: TERCEnsemblGeneIds (GRCh38): ENSG00000270141
EnsemblGeneIds (GRCh37): ENSG00000270141
OMIM: 602322, Gene2Phenotype
TERC is in 15 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- Melbourne Genomics Health Alliance Immunology Flagship
- OMIM
- 602322
- Clinvar variants
- Variants in TERC
- Penetrance
- None
- Panels with this gene
-
- Haematological malignancies cancer susceptibility
- Cytopenia - NOT Fanconi anaemia
- Pulmonary fibrosis familial
- Familial pulmonary fibrosis
- Cytopenias and congenital anaemias
- COVID-19 research
- Childhood solid tumours
- Haematological malignancies for rare disease
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Inherited predisposition to acute myeloid leukaemia (AML)
- Ductal plate malformation
- Pigmentary skin disorders
- Adult solid tumours cancer susceptibility
- DDG2P
- Polycystic liver disease
History Filter Activity
Created, Added New Source, Set mode of inheritance
Rebecca Foulger (Genomics England curator)gene: TERC was added gene: TERC was added to Immunological disorders_SuperPanel_PanelAppAustralia. Sources: Melbourne Genomics Health Alliance Immunology Flagship,Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: TERC was set to Unknown