======= BNIP3L ======= == Gene Information == * **Official Symbol**: BNIP3L * **Official Name**: BCL2 interacting protein 3 like * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=665|665]] * **UniProt**: [[https://www.uniprot.org/uniprot/O60238|O60238]] * **Interactions**: [[https://thebiogrid.org/search.php?search=BNIP3L&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20BNIP3L|Open PubMed]] * **OMIM**: [[https://omim.org/entry/605368|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Induces apoptosis. Interacts with viral and cellular anti-apoptosis proteins. Can overcome the suppressors BCL-2 and BCL-XL, although high levels of BCL-XL expression will inhibit apoptosis. Inhibits apoptosis induced by BNIP3. Involved in mitochondrial quality control via its interaction with SPATA18/MIEAP: in response to mitochondrial damage, participates in mitochondrial protein catabolic process (also named MALM) leading to the degradation of damaged proteins inside mitochondria. The physical interaction of SPATA18/MIEAP, BNIP3 and BNIP3L/NIX at the mitochondrial outer membrane regulates the opening of a pore in the mitochondrial double membrane in order to mediate the translocation of lysosomal proteins from the cytoplasm to the mitochondrial matrix. May function as a tumor suppressor. {ECO:0000269|PubMed:10381623, ECO:0000269|PubMed:21264228}. |BNIP3| |mitochondrial protein catabolic process| |intrinsic component of membrane| |negative regulation of mitochondrial membrane potential| |negative regulation of membrane potential| |mitochondrial outer membrane permeabilization| |lamin binding| |positive regulation of mitochondrial membrane permeability involved in apoptotic process| |mitochondrial outer membrane permeabilization involved in programmed cell death| |positive regulation of mitochondrial membrane permeability| |positive regulation of membrane permeability| |regulation of mitochondrial membrane permeability involved in apoptotic process| |regulation of autophagy of mitochondrion| |regulation of protein targeting to mitochondrion| |apoptotic mitochondrial changes| |positive regulation of macroautophagy| |regulation of mitochondrial membrane potential| |regulation of mitochondrial membrane permeability| |regulation of establishment of protein localization to mitochondrion| |regulation of membrane permeability| |regulation of protein targeting| |positive regulation of autophagy| |mitochondrial membrane organization| |mitochondrial outer membrane| |regulation of macroautophagy| |nuclear envelope| |regulation of mitochondrion organization| |cellular response to hypoxia| |defense response to virus| |cellular response to decreased oxygen levels| |mitochondrial transport| |cellular response to oxygen levels| |regulation of intracellular protein transport| |response to virus| |apoptotic signaling pathway| |regulation of autophagy| |response to hypoxia| |regulation of intracellular transport| |response to decreased oxygen levels| |positive regulation of cellular catabolic process| |response to oxygen levels| |nuclear speck| |regulation of membrane potential| |positive regulation of catabolic process| |mitochondrion organization| |protein heterodimerization activity| |regulation of cellular protein localization| |cellular protein catabolic process| |positive regulation of apoptotic process| |positive regulation of programmed cell death| |protein catabolic process| |positive regulation of cell death| |viral process| |regulation of protein transport| |regulation of peptide transport| |regulation of establishment of protein localization| |symbiotic process| |interspecies interaction between organisms| |regulation of cellular catabolic process| |membrane organization| |protein homodimerization activity| |negative regulation of apoptotic process| |negative regulation of programmed cell death| |cellular macromolecule catabolic process| |regulation of cellular localization| |apoptotic process| |defense response to other organism| |negative regulation of cell death| |regulation of catabolic process| |endoplasmic reticulum| |regulation of protein localization| |macromolecule catabolic process| |programmed cell death| |organonitrogen compound catabolic process| |identical protein binding| |cell death| |immune effector process| |response to abiotic stimulus| |mitochondrion| |regulation of organelle organization| |response to other organism| |response to external biotic stimulus| |response to biotic stimulus| |defense response| |regulation of apoptotic process| |regulation of programmed cell death| |regulation of cell death| |cellular response to stress| |organic substance catabolic process| |cellular catabolic process| |regulation of transport| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp48|Mubritinib 0.2μM R01 exp48]]|-1.71| |[[:results:exp317|Geldanamycin 0.015 to 0.05μM on day4 R07 exp317]]|1.71| ^Gene^Correlation^ |[[:human genes:r:rrm1|RRM1]]|0.602| Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 18527 * **Expression level (log2 read counts)**: 4.93 {{:chemogenomics:nalm6 dist.png?nolink |}}