TERF2
Gene Ontology Biological Process
- in utero embryonic development [IMP]
- negative regulation of telomere maintenance [ISO]
- positive regulation of telomere maintenance [IDA, IMP]
- protection from non-homologous end joining at telomere [IDA, IMP, ISO]
- protein localization to chromosome, telomeric region [ISO]
- telomere capping [ISO]
- telomere maintenance [IMP, ISO]
- telomere maintenance via telomere shortening [IBA]
- telomeric loop formation [IBA, ISO]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
POT1B
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Phenotypic Enhancement
A genetic interaction is inferred when mutation or overexpression of one gene results in enhancement of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.
Publication
TRF2-mediated telomere protection is dispensable in pluripotent stem cells.
In mammals, telomere protection is mediated by the essential protein TRF2, which binds chromosome ends and ensures genome integrity1,2. TRF2 depletion results in end-to-end chromosome fusions in all cell types that have been tested so far. Here we find that TRF2 is dispensable for the proliferation and survival of mouse embryonic stem (ES) cells. Trf2-/- (also known as Terf2) ES ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: abnormal telomere length (MP:0003155)
Additional Notes
- CRISPR method
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
TERF2 POT1B | Negative Genetic Negative Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a more severe fitness defect or lethality under a given condition. This term is reserved for high or low throughput studies with scores. | Low | - | BioGRID | 3515388 | |
TERF2 POT1B | Synthetic Lethality Synthetic Lethality A genetic interaction is inferred when mutations or deletions in separate genes, each of which alone causes a minimal phenotype, result in lethality when combined in the same cell under a given condition. | Low | - | BioGRID | 3515400 |
Curated By
- BioGRID