BAIT
FITM2
AI414861, D930001I22Rik, Fit2, RP23-36P22.6
fat storage-inducing transmembrane protein 2
GO Process (7)
GO Function (0)
GO Component (4)
Gene Ontology Biological Process
Gene Ontology Cellular Component
Mus musculus
PREY
STOML2
0610038F01Rik, MSLP2, SLP-2, RP23-124L1.8
stomatin (Epb7.2)-like 2
GO Process (15)
GO Function (1)
GO Component (11)
Gene Ontology Biological Process
- CD4-positive, alpha-beta T cell activation [IMP]
- T cell receptor signaling pathway [ISO]
- cellular calcium ion homeostasis [ISO]
- interleukin-2 production [IMP]
- lipid localization [IMP]
- mitochondrial ATP synthesis coupled proton transport [IMP, ISO]
- mitochondrial calcium ion transport [ISO]
- mitochondrial protein processing [IMP]
- mitochondrion localization [IMP]
- mitochondrion organization [ISO]
- positive regulation of cardiolipin metabolic process [ISO]
- positive regulation of mitochondrial DNA replication [ISO]
- positive regulation of mitochondrial membrane potential [ISO]
- protein oligomerization [ISO]
- stress-induced mitochondrial fusion [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- COP9 signalosome [ISO]
- T cell receptor complex [ISO]
- actin cytoskeleton [ISO]
- cell [IMP]
- extrinsic component of plasma membrane [IDA, ISO]
- immunological synapse [ISO]
- intracellular [IMP]
- membrane raft [ISO]
- mitochondrial inner membrane [IDA, ISO]
- mitochondrial intermembrane space [ISO]
- mitochondrion [IDA, IMP]
Mus musculus
Positive Genetic
Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a less severe fitness defect than expected under a given condition. This term is reserved for high or low throughput studies with scores.
Publication
Functional genomic landscape of cancer-intrinsic evasion of killing by T cells.
The genetic circuits that allow cancer cells to evade destruction by the host immune system remain poorly understood1-3. Here, to identify a phenotypically robust core set of genes and pathways that enable cancer cells to evade killing mediated by cytotoxic TÂ lymphocytes (CTLs), we performed genome-wide CRISPR screens across a panel of genetically diverse mouse cancer cell lines that were cultured ... [more]
Nature Oct. 01, 2020; 586(7827);120-126 [Pubmed: 32968282]
Throughput
- Low Throughput
Ontology Terms
- phenotype: increased cell proliferation (MP:0000351)
Additional Notes
- CRISPR GI screen
- Cell Line: Renca
- Experimental Setup: Cytokine Exposure: IFNgamma (10ng/ml)
- GIST: A-phenotypic positive genetic interaction
- Library: mTKO
- Significance Threshold: FDR<0.05
Curated By
- BioGRID