======= DHRS2 ======= == Gene Information == * **Official Symbol**: DHRS2 * **Official Name**: dehydrogenase/reductase 2 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=10202|10202]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q13268|Q13268]] * **Interactions**: [[https://thebiogrid.org/search.php?search=DHRS2&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20DHRS2|Open PubMed]] * **OMIM**: [[https://omim.org/entry/615194|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Displays NADPH-dependent dicarbonyl reductase activity in vitro with 3,4-Hexanedione, 2,3-Heptanedione and 1-Phenyl-1,2- propanedione as substrates. No reductase activity is displayed in vitro with steroids, retinoids and sugars as substrates. Attenuates MDM2-mediated p53/TP53 degradation, leading to p53/TP53 stabilization and increased transcription activity, resulting in the accumulation of MDM2 and CDKN1A/p21. {ECO:0000269|PubMed:16685466, ECO:0000269|PubMed:20547751}. |KR| |adh short| |carbonyl reductase (NADPH) activity| |myeloid dendritic cell differentiation| |myeloid dendritic cell activation| |C21-steroid hormone metabolic process| |dendritic cell differentiation| |myeloid leukocyte differentiation| |cellular hormone metabolic process| |nuclear envelope| |hormone metabolic process| |myeloid cell differentiation| |cellular response to oxidative stress| |steroid metabolic process| |leukocyte differentiation| |mitochondrial matrix| |response to oxidative stress| |response to toxic substance| |regulation of hormone levels| |hemopoiesis| |myeloid leukocyte activation| |hematopoietic or lymphoid organ development| |immune system development| |negative regulation of cell population proliferation| |negative regulation of apoptotic process| |negative regulation of programmed cell death| |leukocyte activation| |oxidation-reduction process| |negative regulation of cell death| |cell activation| |lipid metabolic process| |mitochondrion| |regulation of apoptotic process| |regulation of programmed cell death| |regulation of cell population proliferation| |regulation of cell death| |cellular response to stress| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp210|LB-100 2μM R05 exp210]]|-1.72| No correlation found to any other genes in chemogenomics. 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**: 13605 * **Expression level (log2 read counts)**: 2.44 {{:chemogenomics:nalm6 dist.png?nolink |}}