OGT Gene

HGNC Family Glycosyltransferases, Tetratricopeptide repeat domain containing (TTC)
Name O-linked N-acetylglucosamine (GlcNAc) transferase
Description This gene encodes a glycosyltransferase that catalyzes the addition of a single N-acetylglucosamine in O-glycosidic linkage to serine or threonine residues. Since both phosphorylation and glycosylation compete for similar serine or threonine residues, the two processes may compete for sites, or they may alter the substrate specificity of nearby sites by steric or electrostatic effects. The protein contains multiple tetratricopeptide repeats that are required for optimal recognition of substrates. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nO‑GlcNAc transferase (OGT) is a multifaceted enzyme that catalyzes the addition of N‑acetylglucosamine to serine and threonine residues on numerous intracellular proteins. Structural and mechanistic studies have revealed that OGT adopts a fold comprising tandem tetratricopeptide repeats and two Rossmann‐like domains that form a superhelical groove for substrate binding. High‐resolution crystallographic snapshots and kinetic analyses have uncovered unique features of the enzyme’s donor recognition and peptide substrate specificity, establishing the basis for its catalytic mechanism and providing insight into how subtle changes in the active site can impact overall activity."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "6"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn response to metabolic cues, OGT functions as a nutrient sensor that integrates glucose availability and hexosamine flux into widespread post‑translational modifications. Under conditions such as glucose deprivation, increased OGT mRNA and protein levels drive an elevation in global O‑GlcNAcylation, thereby linking cellular energy status to diverse signaling cascades. Reviews of these phenomena further underscore OGT’s role in coupling nutrient status to key regulatory processes in normal physiology."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "7", "end_ref": "10"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its metabolic sensing role, OGT critically modulates epigenetic and cell cycle regulatory networks. OGT directly interacts with the ten‐eleven translocation (TET) family of dioxygenases, promoting histone O‑GlcNAcylation and thereby influencing chromatin structure and gene transcription. In addition, its capacity to proteolytically process host cell factor‑1 (HCF‑1) and to coordinate with mitotic kinases underscores its involvement in proper cell division and chromosomal segregation."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "11", "end_ref": "15"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the context of cancer, aberrant OGT expression and activity have been linked to oncogenic signaling and metabolic reprogramming. In prostate and other cancers, increased OGT expression stabilizes key oncogenic factors such as c‑Myc and FoxM1 and augments pro‑tumorigenic pathways including the pentose phosphate pathway via glycosylation of enzymes like glucose‑6‑phosphate dehydrogenase. Moreover, OGT is integrated into Polycomb repressive complexes, further impacting gene silencing programs during tumor progression."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "16", "end_ref": "21"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nOGT also regulates key stress response pathways, including autophagy, through modification of factors such as the SNARE protein SNAP‑29, thereby promoting autophagic flux during nutrient deprivation. In parallel, O‑GlcNAcylation of regulatory proteins like KEAP1 modulates the stability of the transcription factor NRF2, linking OGT activity to redox homeostasis. These alterations have implications for chemoresistance in cancers, as diminished OGT expression correlates with altered autophagy and drug responsiveness."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "22", "end_ref": "26"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFinally, emerging evidence underscores the importance of OGT in neurodevelopment and placental function. Variations in placental OGT levels have been linked to maternal stress and sex‑biased outcomes in neurodevelopmental disorders, while mutations in the OGT gene itself are associated with X‑linked intellectual disability. These findings highlight OGT’s broader significance in developmental programming and disease predisposition."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "27", "end_ref": "29"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Carlos Martinez-Fleites, Matthew S Macauley, Yuan He, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Structure of an O-GlcNAc transferase homolog provides insight into intracellular glycosylation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Struct Mol Biol (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nsmb.1443"}], "href": "https://doi.org/10.1038/nsmb.1443"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18536723"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18536723"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Michael B Lazarus, Yunsun Nam, Jiaoyang Jiang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Structure of human O-GlcNAc transferase and its complex with a peptide substrate."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nature (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nature09638"}], "href": "https://doi.org/10.1038/nature09638"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21240259"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21240259"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "David L Shen, Tracey M Gloster, Scott A Yuzwa, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Insights into O-linked N-acetylglucosamine ([0-9]O-GlcNAc) processing and dynamics through kinetic analysis of O-GlcNAc transferase and O-GlcNAcase activity on protein substrates."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M111.310664"}], "href": "https://doi.org/10.1074/jbc.M111.310664"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22311971"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22311971"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Michael B Lazarus, Jiaoyang Jiang, Tracey M Gloster, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Structural snapshots of the reaction coordinate for O-GlcNAc transferase."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Chem Biol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nchembio.1109"}], "href": "https://doi.org/10.1038/nchembio.1109"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23103939"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23103939"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Marianne Schimpl, Xiaowei Zheng, Vladimir S Borodkin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAc transferase invokes nucleotide sugar pyrophosphate participation in catalysis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Chem Biol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nchembio.1108"}], "href": "https://doi.org/10.1038/nchembio.1108"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23103942"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23103942"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Shalini Pathak, Jana Alonso, Marianne Schimpl, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The active site of O-GlcNAc transferase imposes constraints on substrate sequence."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Struct Mol Biol (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nsmb.3063"}], "href": "https://doi.org/10.1038/nsmb.3063"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26237509"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26237509"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Donald A McClain, William A Lubas, Robert C Cooksey, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Altered glycan-dependent signaling induces insulin resistance and hyperleptinemia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.152346899"}], "href": "https://doi.org/10.1073/pnas.152346899"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12136128"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12136128"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Rodrick P Taylor, Glendon J Parker, Mark W Hazel, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Glucose deprivation stimulates O-GlcNAc modification of proteins through up-regulation of O-linked N-acetylglucosaminyltransferase."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M707328200"}], "href": "https://doi.org/10.1074/jbc.M707328200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18174169"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18174169"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Michelle R Bond, John A Hanover "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAc cycling: a link between metabolism and chronic disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Annu Rev Nutr (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1146/annurev-nutr-071812-161240"}], "href": "https://doi.org/10.1146/annurev-nutr-071812-161240"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23642195"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23642195"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Lewis J Watson, Heberty T Facundo, Gladys A Ngoh, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-linked β-N-acetylglucosamine transferase is indispensable in the failing heart."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1001907107"}], "href": "https://doi.org/10.1073/pnas.1001907107"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20876116"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20876116"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Qiang Chen, Yibin Chen, Chunjing Bian, et al. "}, {"type": "b", "children": [{"type": "t", "text": "TET2 promotes histone O-GlcNAcylation during gene transcription."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nature (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nature11742"}], "href": "https://doi.org/10.1038/nature11742"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23222540"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23222540"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Michael B Lazarus, Jiaoyang Jiang, Vaibhav Kapuria, et al. "}, {"type": "b", "children": [{"type": "t", "text": "HCF-1 is cleaved in the active site of O-GlcNAc transferase."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Science (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1126/science.1243990"}], "href": "https://doi.org/10.1126/science.1243990"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24311690"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24311690"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Zebulon G Levine, Suzanne Walker "}, {"type": "b", "children": [{"type": "t", "text": "The Biochemistry of O-GlcNAc Transferase: Which Functions Make It Essential in Mammalian Cells?"}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Annu Rev Biochem (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1146/annurev-biochem-060713-035344"}], "href": "https://doi.org/10.1146/annurev-biochem-060713-035344"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27294441"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27294441"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Kaoru Sakabe, Gerald W Hart "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAc transferase regulates mitotic chromatin dynamics."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M110.158170"}], "href": "https://doi.org/10.1074/jbc.M110.158170"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20805223"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20805223"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Chad Slawson, T Lakshmanan, Spencer Knapp, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A mitotic GlcNAcylation/phosphorylation signaling complex alters the posttranslational state of the cytoskeletal protein vimentin."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Cell (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1091/mbc.e07-11-1146"}], "href": "https://doi.org/10.1091/mbc.e07-11-1146"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18653473"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18653473"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Anna Krześlak, Ewa Forma, Magdalena Bernaciak, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Gene expression of O-GlcNAc cycling enzymes in human breast cancers."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Clin Exp Med (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s10238-011-0138-5"}], "href": "https://doi.org/10.1007/s10238-011-0138-5"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21567137"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21567137"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Harri M Itkonen, Sarah Minner, Ingrid J Guldvik, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAc transferase integrates metabolic pathways to regulate the stability of c-MYC in human prostate cancer cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Res (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1158/0008-5472.CAN-13-0549"}], "href": "https://doi.org/10.1158/0008-5472.CAN-13-0549"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23720054"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23720054"}]}, {"type": "r", "ref": 18, "children": [{"type": "t", "text": "Xiongjian Rao, Xiaotao Duan, Weimin Mao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAcylation of G6PD promotes the pentose phosphate pathway and tumor growth."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncomms9468"}], "href": "https://doi.org/10.1038/ncomms9468"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26399441"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26399441"}]}, {"type": "r", "ref": 19, "children": [{"type": "t", "text": "Stefan Burén, Ana L Gomes, Ana Teijeiro, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Regulation of OGT by URI in Response to Glucose Confers c-MYC-Dependent Survival Mechanisms."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Cell (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ccell.2016.06.023"}], "href": "https://doi.org/10.1016/j.ccell.2016.06.023"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27505673"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27505673"}]}, {"type": "r", "ref": 20, "children": [{"type": "t", "text": "Simon Hauri, Federico Comoglio, Makiko Seimiya, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A High-Density Map for Navigating the Human Polycomb Complexome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.celrep.2016.08.096"}], "href": "https://doi.org/10.1016/j.celrep.2016.08.096"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27705803"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27705803"}]}, {"type": "r", "ref": 21, "children": [{"type": "t", "text": "Weiqi Xu, Xiang Zhang, Jian-Lin Wu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAc transferase promotes fatty liver-associated liver cancer through inducing palmitic acid and activating endoplasmic reticulum stress."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Hepatol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jhep.2017.03.017"}], "href": "https://doi.org/10.1016/j.jhep.2017.03.017"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28347804"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28347804"}]}, {"type": "r", "ref": 22, "children": [{"type": "t", "text": "Zahra Kazemi, Hana Chang, Sarah Haserodt, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-linked beta-N-acetylglucosamine (O-GlcNAc) regulates stress-induced heat shock protein expression in a GSK-3beta-dependent manner."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M110.131102"}], "href": "https://doi.org/10.1074/jbc.M110.131102"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20926391"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20926391"}]}, {"type": "r", "ref": 23, "children": [{"type": "t", "text": "Bin Guo, Qianqian Liang, Lin Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAc-modification of SNAP-29 regulates autophagosome maturation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Cell Biol (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncb3066"}], "href": "https://doi.org/10.1038/ncb3066"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25419848"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25419848"}]}, {"type": "r", "ref": 24, "children": [{"type": "t", "text": "Po-Han Chen, Timothy J Smith, Jianli Wu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Glycosylation of KEAP1 links nutrient sensing to redox stress signaling."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO J (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.15252/embj.201696113"}], "href": "https://doi.org/10.15252/embj.201696113"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28663241"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28663241"}]}, {"type": "r", "ref": 25, "children": [{"type": "t", "text": "Tianliang Li, Xinghui Li, Kuldeep S Attri, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAc Transferase Links Glucose Metabolism to MAVS-Mediated Antiviral Innate Immunity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Host Microbe (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.chom.2018.11.001"}], "href": "https://doi.org/10.1016/j.chom.2018.11.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30543776"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30543776"}]}, {"type": "r", "ref": 26, "children": [{"type": "t", "text": "Fuxing Zhou, Xiaoshan Yang, Hang Zhao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Down-regulation of OGT promotes cisplatin resistance by inducing autophagy in ovarian cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Theranostics (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.7150/thno.27806"}], "href": "https://doi.org/10.7150/thno.27806"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30555541"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30555541"}]}, {"type": "r", "ref": 27, "children": [{"type": "t", "text": "Christopher L Howerton, Christopher P Morgan, David B Fischer, et al. "}, {"type": "b", "children": [{"type": "t", "text": "O-GlcNAc transferase (OGT) as a placental biomarker of maternal stress and reprogramming of CNS gene transcription in development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1300065110"}], "href": "https://doi.org/10.1073/pnas.1300065110"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23487789"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23487789"}]}, {"type": "r", "ref": 28, "children": [{"type": "t", "text": "Krithika Vaidyanathan, Tejasvi Niranjan, Nithya Selvan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification and characterization of a missense mutation in the "}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "O"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": "-linked β-"}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "N"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": "-acetylglucosamine ("}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "O"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": "-GlcNAc) transferase gene that segregates with X-linked intellectual disability."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M116.771030"}], "href": "https://doi.org/10.1074/jbc.M116.771030"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28302723"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28302723"}]}, {"type": "r", "ref": 29, "children": [{"type": "t", "text": "Bridget M Nugent, Carly M O'Donnell, C Neill Epperson, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Placental H3K27me3 establishes female resilience to prenatal insults."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41467-018-04992-1"}], "href": "https://doi.org/10.1038/s41467-018-04992-1"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29967448"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29967448"}]}]}]}
Synonyms MRX106, OGT1, HINCUT-1, HRNT1, O-GLCNAC
Proteins OGT1_HUMAN
NCBI Gene ID 8473
API
Download Associations
Predicted Functions View OGT's ARCHS4 Predicted Functions.
Co-expressed Genes View OGT's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View OGT's ARCHS4 Predicted Functions.

Functional Associations

OGT has 10,722 functional associations with biological entities spanning 8 categories (molecular profile, organism, chemical, disease, phenotype or trait, functional term, phrase or reference, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 134 datasets.

Click the + buttons to view associations for OGT from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
Achilles Cell Line Gene Essentiality Profiles cell lines with fitness changed by OGT gene knockdown relative to other cell lines from the Achilles Cell Line Gene Essentiality Profiles dataset.
Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles tissues with high or low expression of OGT gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles tissue samples with high or low expression of OGT gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray tissue samples with high or low expression of OGT gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq tissue samples with high or low expression of OGT gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles tissues with high or low expression of OGT gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
BioGPS Cell Line Gene Expression Profiles cell lines with high or low expression of OGT gene relative to other cell lines from the BioGPS Cell Line Gene Expression Profiles dataset.
BioGPS Human Cell Type and Tissue Gene Expression Profiles cell types and tissues with high or low expression of OGT gene relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
BioGPS Mouse Cell Type and Tissue Gene Expression Profiles cell types and tissues with high or low expression of OGT gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
Carcinogenome Chemical Perturbation Carcinogenicity Signatures small molecule perturbations changing expression of OGT gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
CCLE Cell Line Gene CNV Profiles cell lines with high or low copy number of OGT gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
CCLE Cell Line Gene Expression Profiles cell lines with high or low expression of OGT gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
CCLE Cell Line Proteomics Cell lines associated with OGT protein from the CCLE Cell Line Proteomics dataset.
CellMarker Gene-Cell Type Associations cell types associated with OGT gene from the CellMarker Gene-Cell Type Associations dataset.
ChEA Transcription Factor Binding Site Profiles transcription factor binding site profiles with transcription factor binding evidence at the promoter of OGT gene from the CHEA Transcription Factor Binding Site Profiles dataset.
ChEA Transcription Factor Targets transcription factors binding the promoter of OGT gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
ChEA Transcription Factor Targets 2022 transcription factors binding the promoter of OGT gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
ClinVar Gene-Phenotype Associations 2025 phenotypes associated with OGT gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CMAP Signatures of Differentially Expressed Genes for Small Molecules small molecule perturbations changing expression of OGT gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
COMPARTMENTS Curated Protein Localization Evidence Scores cellular components containing OGT protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
COMPARTMENTS Curated Protein Localization Evidence Scores 2025 cellular components containing OGT protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
COMPARTMENTS Experimental Protein Localization Evidence Scores cellular components containing OGT protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 cellular components containing OGT protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.
COMPARTMENTS Text-mining Protein Localization Evidence Scores cellular components co-occuring with OGT protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 cellular components co-occuring with OGT protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
CORUM Protein Complexes protein complexs containing OGT protein from the CORUM Protein Complexes dataset.
COSMIC Cell Line Gene CNV Profiles cell lines with high or low copy number of OGT gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
COSMIC Cell Line Gene Mutation Profiles cell lines with OGT gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
CTD Gene-Chemical Interactions chemicals interacting with OGT gene/protein from the curated CTD Gene-Chemical Interactions dataset.
CTD Gene-Disease Associations diseases associated with OGT gene/protein from the curated CTD Gene-Disease Associations dataset.
DeepCoverMOA Drug Mechanisms of Action small molecule perturbations with high or low expression of OGT protein relative to other small molecule perturbations from the DeepCoverMOA Drug Mechanisms of Action dataset.
DISEASES Text-mining Gene-Disease Association Evidence Scores diseases co-occuring with OGT gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 diseases co-occuring with OGT gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
DisGeNET Gene-Disease Associations diseases associated with OGT gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
DisGeNET Gene-Phenotype Associations phenotypes associated with OGT gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.
ENCODE Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at OGT gene from the ENCODE Histone Modification Site Profiles dataset.
ENCODE Transcription Factor Binding Site Profiles transcription factor binding site profiles with transcription factor binding evidence at the promoter of OGT gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of OGT gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
ESCAPE Omics Signatures of Genes and Proteins for Stem Cells PubMedIDs of publications reporting gene signatures containing OGT from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.
GAD Gene-Disease Associations diseases associated with OGT gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
GAD High Level Gene-Disease Associations diseases associated with OGT gene in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.
GDSC Cell Line Gene Expression Profiles cell lines with high or low expression of OGT gene relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.
GeneRIF Biological Term Annotations biological terms co-occuring with OGT gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
GeneSigDB Published Gene Signatures PubMedIDs of publications reporting gene signatures containing OGT from the GeneSigDB Published Gene Signatures dataset.
GEO Signatures of Differentially Expressed Genes for Diseases disease perturbations changing expression of OGT gene from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
GEO Signatures of Differentially Expressed Genes for Gene Perturbations gene perturbations changing expression of OGT gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
GEO Signatures of Differentially Expressed Genes for Kinase Perturbations kinase perturbations changing expression of OGT gene from the GEO Signatures of Differentially Expressed Genes for Kinase Perturbations dataset.
GEO Signatures of Differentially Expressed Genes for Small Molecules small molecule perturbations changing expression of OGT gene from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations transcription factor perturbations changing expression of OGT gene from the GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations dataset.
GEO Signatures of Differentially Expressed Genes for Viral Infections virus perturbations changing expression of OGT gene from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.
GO Biological Process Annotations 2015 biological processes involving OGT gene from the curated GO Biological Process Annotations 2015 dataset.
GO Biological Process Annotations 2023 biological processes involving OGT gene from the curated GO Biological Process Annotations 2023 dataset.
GO Biological Process Annotations 2025 biological processes involving OGT gene from the curated GO Biological Process Annotations2025 dataset.
GO Cellular Component Annotations 2015 cellular components containing OGT protein from the curated GO Cellular Component Annotations 2015 dataset.
GO Cellular Component Annotations 2023 cellular components containing OGT protein from the curated GO Cellular Component Annotations 2023 dataset.
GO Cellular Component Annotations 2025 cellular components containing OGT protein from the curated GO Cellular Component Annotations 2025 dataset.
GO Molecular Function Annotations 2015 molecular functions performed by OGT gene from the curated GO Molecular Function Annotations 2015 dataset.
GO Molecular Function Annotations 2023 molecular functions performed by OGT gene from the curated GO Molecular Function Annotations 2023 dataset.
GO Molecular Function Annotations 2025 molecular functions performed by OGT gene from the curated GO Molecular Function Annotations 2025 dataset.
GTEx Tissue Gene Expression Profiles tissues with high or low expression of OGT gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.
GTEx Tissue Gene Expression Profiles 2023 tissues with high or low expression of OGT gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.
GTEx Tissue Sample Gene Expression Profiles tissue samples with high or low expression of OGT gene relative to other tissue samples from the GTEx Tissue Sample Gene Expression Profiles dataset.
GTEx Tissue-Specific Aging Signatures tissue samples with high or low expression of OGT gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset.
GWAS Catalog SNP-Phenotype Associations 2025 phenotypes associated with OGT gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
GWASdb SNP-Disease Associations diseases associated with OGT gene in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
GWASdb SNP-Phenotype Associations phenotypes associated with OGT gene in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
Heiser et al., PNAS, 2011 Cell Line Gene Expression Profiles cell lines with high or low expression of OGT gene relative to other cell lines from the Heiser et al., PNAS, 2011 Cell Line Gene Expression Profiles dataset.
HMDB Metabolites of Enzymes interacting metabolites for OGT protein from the curated HMDB Metabolites of Enzymes dataset.
HPA Cell Line Gene Expression Profiles cell lines with high or low expression of OGT gene relative to other cell lines from the HPA Cell Line Gene Expression Profiles dataset.
HPA Tissue Gene Expression Profiles tissues with high or low expression of OGT gene relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.
HPA Tissue Protein Expression Profiles tissues with high or low expression of OGT protein relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.
HPA Tissue Sample Gene Expression Profiles tissue samples with high or low expression of OGT gene relative to other tissue samples from the HPA Tissue Sample Gene Expression Profiles dataset.
Hub Proteins Protein-Protein Interactions interacting hub proteins for OGT from the curated Hub Proteins Protein-Protein Interactions dataset.
HuGE Navigator Gene-Phenotype Associations phenotypes associated with OGT gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
HumanCyc Pathways pathways involving OGT protein from the HumanCyc Pathways dataset.
InterPro Predicted Protein Domain Annotations protein domains predicted for OGT protein from the InterPro Predicted Protein Domain Annotations dataset.
JASPAR Predicted Human Transcription Factor Targets 2025 transcription factors regulating expression of OGT gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Human Transcription Factor Targets dataset.
JASPAR Predicted Mouse Transcription Factor Targets 2025 transcription factors regulating expression of OGT gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of OGT gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset.
KEA Substrates of Kinases kinases that phosphorylate OGT protein from the curated KEA Substrates of Kinases dataset.
KEGG Pathways pathways involving OGT protein from the KEGG Pathways dataset.
KEGG Pathways 2026 pathways involving OGT protein from the KEGG Pathways 2026 dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of OGT gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles cell lines with high or low expression of OGT gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles cell lines with OGT gene mutations from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles dataset.
KnockTF Gene Expression Profiles with Transcription Factor Perturbations transcription factor perturbations changing expression of OGT gene from the KnockTF Gene Expression Profiles with Transcription Factor Perturbations dataset.
LINCS L1000 CMAP Chemical Perturbation Consensus Signatures small molecule perturbations changing expression of OGT gene from the LINCS L1000 CMAP Chemical Perturbations Consensus Signatures dataset.
LINCS L1000 CMAP CRISPR Knockout Consensus Signatures gene perturbations changing expression of OGT gene from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset.
LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules small molecule perturbations changing expression of OGT gene from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
LOCATE Curated Protein Localization Annotations cellular components containing OGT protein in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.
LOCATE Predicted Protein Localization Annotations cellular components predicted to contain OGT protein from the LOCATE Predicted Protein Localization Annotations dataset.
MGI Mouse Phenotype Associations 2023 phenotypes of transgenic mice caused by OGT gene mutations from the MGI Mouse Phenotype Associations 2023 dataset.
MiRTarBase microRNA Targets microRNAs targeting OGT gene in low- or high-throughput microRNA targeting studies from the MiRTarBase microRNA Targets dataset.
MotifMap Predicted Transcription Factor Targets transcription factors regulating expression of OGT gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.
MoTrPAC Rat Endurance Exercise Training tissue samples with high or low expression of OGT gene relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
MPO Gene-Phenotype Associations phenotypes of transgenic mice caused by OGT gene mutations from the MPO Gene-Phenotype Associations dataset.
MSigDB Cancer Gene Co-expression Modules co-expressed genes for OGT from the MSigDB Cancer Gene Co-expression Modules dataset.
MW Enzyme Metabolite Associations interacting metabolites for OGT protein from the MW Gene Metabolite Associations dataset.
NIBR DRUG-seq U2OS MoA Box Gene Expression Profiles drug perturbations changing expression of OGT gene from the NIBR DRUG-seq U2OS MoA Box dataset.
NURSA Protein Complexes protein complexs containing OGT protein recovered by IP-MS from the NURSA Protein Complexes dataset.
Pathway Commons Protein-Protein Interactions interacting proteins for OGT from the Pathway Commons Protein-Protein Interactions dataset.
PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations gene perturbations changing expression of OGT gene from the PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
PerturbAtlas Signatures of Differentially Expressed Genes for Mouse Gene Perturbations gene perturbations changing expression of OGT gene from the PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
PFOCR Pathway Figure Associations 2023 pathways involving OGT protein from the PFOCR Pathway Figure Associations 2023 dataset.
PFOCR Pathway Figure Associations 2024 pathways involving OGT protein from the Wikipathways PFOCR 2024 dataset.
Phosphosite Textmining Biological Term Annotations biological terms co-occuring with OGT protein in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
PhosphoSitePlus Substrates of Kinases kinases that phosphorylate OGT protein from the curated PhosphoSitePlus Substrates of Kinases dataset.
ProteomicsDB Cell Type and Tissue Protein Expression Profiles cell types and tissues with high or low expression of OGT protein relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset.
Reactome Pathways 2014 pathways involving OGT protein from the Reactome Pathways dataset.
Reactome Pathways 2024 pathways involving OGT protein from the Reactome Pathways 2024 dataset.
Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures gene perturbations changing expression of OGT gene from the Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures dataset.
Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures gene perturbations changing expression of OGT gene from the Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures dataset.
Replogle et al., Cell, 2022 RPE1 Essential Perturb-seq Gene Perturbation Signatures gene perturbations changing expression of OGT gene from the Replogle et al., Cell, 2022 RPE1 Essential Perturb-seq Gene Perturbation Signatures dataset.
Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles cell types and tissues with high or low DNA methylation of OGT gene relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.
Roadmap Epigenomics Cell and Tissue Gene Expression Profiles cell types and tissues with high or low expression of OGT gene relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue Gene Expression Profiles dataset.
Roadmap Epigenomics Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at OGT gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
RummaGEO Drug Perturbation Signatures drug perturbations changing expression of OGT gene from the RummaGEO Drug Perturbation Signatures dataset.
RummaGEO Gene Perturbation Signatures gene perturbations changing expression of OGT gene from the RummaGEO Gene Perturbation Signatures dataset.
Sanger Dependency Map Cancer Cell Line Proteomics cell lines associated with OGT protein from the Sanger Dependency Map Cancer Cell Line Proteomics dataset.
Sci-Plex Drug Perturbation Signatures drug perturbations changing expression of OGT gene from the Sci-Plex Drug Perturbation Signatures dataset.
SILAC Phosphoproteomics Signatures of Differentially Phosphorylated Proteins for Drugs drug perturbations changing phosphorylation of OGT protein from the SILAC Phosphoproteomics Signatures of Differentially Phosphorylated Proteins for Drugs dataset.
SynGO Synaptic Gene Annotations synaptic terms associated with OGT gene from the SynGO Synaptic Gene Annotations dataset.
Tahoe Therapeutics Tahoe 100M Perturbation Atlas drug perturbations changing expression of OGT gene from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
TargetScan Predicted Conserved microRNA Targets microRNAs regulating expression of OGT gene predicted using conserved miRNA seed sequences from the TargetScan Predicted Conserved microRNA Targets dataset.
TargetScan Predicted Nonconserved microRNA Targets microRNAs regulating expression of OGT gene predicted using nonconserved miRNA seed sequences from the TargetScan Predicted Nonconserved microRNA Targets dataset.
TCGA Signatures of Differentially Expressed Genes for Tumors tissue samples with high or low expression of OGT gene relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
TISSUES Curated Tissue Protein Expression Evidence Scores tissues with high expression of OGT protein from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
TISSUES Curated Tissue Protein Expression Evidence Scores 2025 tissues with high expression of OGT protein from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
TISSUES Experimental Tissue Protein Expression Evidence Scores tissues with high expression of OGT protein in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 tissues with high expression of OGT protein in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
TISSUES Text-mining Tissue Protein Expression Evidence Scores tissues co-occuring with OGT protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 tissues co-occuring with OGT protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
WikiPathways Pathways 2014 pathways involving OGT protein from the Wikipathways Pathways 2014 dataset.
WikiPathways Pathways 2024 pathways involving OGT protein from the WikiPathways Pathways 2024 dataset.