ITCH Gene

HGNC Family C2 domain containing
Name itchy E3 ubiquitin protein ligase
Description This gene encodes a member of the Nedd4 family of HECT domain E3 ubiquitin ligases. HECT domain E3 ubiquitin ligases transfer ubiquitin from E2 ubiquitin-conjugating enzymes to protein substrates, thus targeting specific proteins for lysosomal degradation. The encoded protein plays a role in multiple cellular processes including erythroid and lymphoid cell differentiation and the regulation of immune responses. Mutations in this gene are a cause of syndromic multisystem autoimmune disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nRecent studies have revealed that circular RNA species derived from the ITCH gene—collectively known as circ‐ITCH—act as tumor suppressors by “sponging” oncogenic microRNAs, thereby preserving or enhancing the expression of the parental ITCH protein. In both bladder and lung cancer, decreased circ‐ITCH levels correlate with enhanced activation of oncogenic pathways such as Wnt/β‐catenin signaling, ultimately promoting tumor progression and malignancy."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nITCH, a HECT‐domain E3 ubiquitin ligase, plays a pivotal role in the ubiquitin–proteasome and lysosomal degradation pathways by targeting a broad spectrum of substrates. It directly ubiquitinates key signaling molecules including the transcriptional regulator p73—thereby controlling cell cycle arrest and apoptosis—and modulators such as Gli1 in Hedgehog signaling and Dishevelled in the Wnt pathway. In addition, ITCH governs the fate of cell‐surface receptors (for example, CXCR4 and occludin), affecting their endocytic trafficking and lysosomal sorting. Moreover, by directing the turnover of critical regulators like LATS1 in Hippo signaling, SMAD7 in TGF‐β signaling, and even Jun and EGFR family proteins, ITCH intricately tunes diverse cellular responses ranging from antiviral immunity to receptor‐mediated downstream signaling."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "4", "end_ref": "24"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nThe activity and stability of ITCH itself are subject to complex regulatory mechanisms that involve interactions with adaptor proteins, post‐translational modifications, and even auto‐ubiquitination. Adaptor factors such as NDFIP proteins relieve ITCH’s autoinhibitory conformation and thereby activate its catalytic function, while regulators like FAM/USP9X and YOD1 modulate ITCH levels through deubiquitination. Genetic deficiency or mutation of ITCH is linked to multisystem autoimmune disease and developmental abnormalities, underscoring its critical physiological role. In addition, ITCH is co‐opted by pathogens—such as adenovirus and Epstein–Barr virus—to facilitate aspects of their life cycle, including viral protein processing and nuclear egress, and it regulates the ubiquitination of oncoproteins (for example, BRAF, AMOT130/YAP, Smad7, Melan‐A, SuFu, FLIP[L], and MAVS) thereby influencing cell survival, apoptosis, and tumorigenesis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "25", "end_ref": "44"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Chengdi Yang, Wenbo Yuan, Xiao Yang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Circular RNA circ-ITCH inhibits bladder cancer progression by sponging miR-17/miR-224 and regulating p21, PTEN expression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cancer (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s12943-018-0771-7"}], "href": "https://doi.org/10.1186/s12943-018-0771-7"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29386015"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29386015"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Li Wan, Lin Zhang, Kai Fan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Circular RNA-ITCH Suppresses Lung Cancer Proliferation via Inhibiting the Wnt/β-Catenin Pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biomed Res Int (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1155/2016/1579490"}], "href": "https://doi.org/10.1155/2016/1579490"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27642589"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27642589"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Yang Li, Yu-Zheng Ge, Luwei Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Circular RNA ITCH: A novel tumor suppressor in multiple cancers."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Life Sci (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.lfs.2019.117176"}], "href": "https://doi.org/10.1016/j.lfs.2019.117176"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31843532"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31843532"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Adriano Marchese, Camilla Raiborg, Francesca Santini, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The E3 ubiquitin ligase AIP4 mediates ubiquitination and sorting of the G protein-coupled receptor CXCR4."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Dev Cell (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/s1534-5807(03)00321-6"}], "href": "https://doi.org/10.1016/s1534-5807(03"}, {"type": "t", "text": "00321-6) PMID: "}, {"type": "a", "children": [{"type": "t", "text": "14602072"}], "href": "https://pubmed.ncbi.nlm.nih.gov/14602072"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Mario Rossi, Vincenzo De Laurenzi, Eliana Munarriz, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The ubiquitin-protein ligase Itch regulates p73 stability."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO J (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.emboj.7600444"}], "href": "https://doi.org/10.1038/sj.emboj.7600444"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15678106"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15678106"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Fuping You, Hui Sun, Xiang Zhou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "PCBP2 mediates degradation of the adaptor MAVS via the HECT ubiquitin ligase AIP4."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Immunol (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ni.1815"}], "href": "https://doi.org/10.1038/ni.1815"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19881509"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19881509"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Lucia Di Marcotullio, Elisabetta Ferretti, Azzura Greco, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Numb is a suppressor of Hedgehog signalling and targets Gli1 for Itch-dependent ubiquitination."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Cell Biol (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncb1510"}], "href": "https://doi.org/10.1038/ncb1510"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17115028"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17115028"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Deepali Bhandari, JoAnn Trejo, Jeffrey L Benovic, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Arrestin-2 interacts with the ubiquitin-protein isopeptide ligase atrophin-interacting protein 4 and mediates endosomal sorting of the chemokine receptor CXCR4."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M705085200"}], "href": "https://doi.org/10.1074/jbc.M705085200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17947233"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17947233"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Andreas Traweger, Deyu Fang, Yun-Cai Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The tight junction-specific protein occludin is a functional target of the E3 ubiquitin-protein ligase itch."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M111384200"}], "href": "https://doi.org/10.1074/jbc.M111384200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "11782481"}], "href": "https://pubmed.ncbi.nlm.nih.gov/11782481"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Patricia Chastagner, Alain Israël, Christel Brou "}, {"type": "b", "children": [{"type": "t", "text": "Itch/AIP4 mediates Deltex degradation through the formation of K29-linked polyubiquitin chains."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO Rep (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.embor.7400822"}], "href": "https://doi.org/10.1038/sj.embor.7400822"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17028573"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17028573"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Zaidoun Salah, Gerry Melino, Rami I Aqeilan "}, {"type": "b", "children": [{"type": "t", "text": "Negative regulation of the Hippo pathway by E3 ubiquitin ligase ITCH is sufficient to promote tumorigenicity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Res (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1158/0008-5472.CAN-10-3516"}], "href": "https://doi.org/10.1158/0008-5472.CAN-10-3516"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21212414"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21212414"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Wei Wei, Meng Li, Jiyong Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The E3 ubiquitin ligase ITCH negatively regulates canonical Wnt signaling by targeting dishevelled protein."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.00251-12"}], "href": "https://doi.org/10.1128/MCB.00251-12"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22826439"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22826439"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Patricia Chastagner, Alain Israël, Christel Brou "}, {"type": "b", "children": [{"type": "t", "text": "AIP4/Itch regulates Notch receptor degradation in the absence of ligand."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0002735"}], "href": "https://doi.org/10.1371/journal.pone.0002735"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18628966"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18628966"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Deyu Fang, Tom K Kerppola "}, {"type": "b", "children": [{"type": "t", "text": "Ubiquitin-mediated fluorescence complementation reveals that Jun ubiquitinated by Itch/AIP4 is localized to lysosomes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.0404445101"}], "href": "https://doi.org/10.1073/pnas.0404445101"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15469925"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15469925"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Wen-Chi Su, Yung-Chia Chen, Chung-Hsin Tseng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Pooled RNAi screen identifies ubiquitin ligase Itch as crucial for influenza A virus release from the endosome during virus entry."}]}, {"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.1312374110"}], "href": "https://doi.org/10.1073/pnas.1312374110"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24101521"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24101521"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "King Ching Ho, Zhonghua Zhou, Yi-Min She, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Itch E3 ubiquitin ligase regulates large tumor suppressor 1 stability [corrected]."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1101273108"}], "href": "https://doi.org/10.1073/pnas.1101273108"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21383157"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21383157"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Rania Mouchantaf, Bilal A Azakir, Peter S McPherson, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The ubiquitin ligase itch is auto-ubiquitylated in vivo and in vitro but is protected from degradation by interacting with the deubiquitylating enzyme FAM/USP9X."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M605959200"}], "href": "https://doi.org/10.1074/jbc.M605959200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17038327"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17038327"}]}, {"type": "r", "ref": 18, "children": [{"type": "t", "text": "L Di Marcotullio, A Greco, D Mazzà, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Numb activates the E3 ligase Itch to control Gli1 function through a novel degradation signal."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncogene (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/onc.2010.394"}], "href": "https://doi.org/10.1038/onc.2010.394"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20818436"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20818436"}]}, {"type": "r", "ref": 19, "children": [{"type": "t", "text": "Pingzhao Zhang, Chenji Wang, Kun Gao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The ubiquitin ligase itch regulates apoptosis by targeting thioredoxin-interacting protein for ubiquitin-dependent degradation."}]}, {"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.M109.063321"}], "href": "https://doi.org/10.1074/jbc.M109.063321"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20068034"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20068034"}]}, {"type": "r", "ref": 20, "children": [{"type": "t", "text": "Zan Chen, Hanjie Jiang, Wei Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A Tunable Brake for HECT Ubiquitin Ligases."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.molcel.2017.03.020"}], "href": "https://doi.org/10.1016/j.molcel.2017.03.020"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28475870"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28475870"}]}, {"type": "r", "ref": 21, "children": [{"type": "t", "text": "Deepali Bhandari, Seth L Robia, Adriano Marchese "}, {"type": "b", "children": [{"type": "t", "text": "The E3 ubiquitin ligase atrophin interacting protein 4 binds directly to the chemokine receptor CXCR4 via a novel WW domain-mediated interaction."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Cell (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1091/mbc.e08-03-0308"}], "href": "https://doi.org/10.1091/mbc.e08-03-0308"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19116316"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19116316"}]}, {"type": "r", "ref": 22, "children": [{"type": "t", "text": "Deepa Sampath, George A Calin, Vinay K Puduvalli, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Specific activation of microRNA106b enables the p73 apoptotic response in chronic lymphocytic leukemia by targeting the ubiquitin ligase Itch for degradation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2008-09-178707"}], "href": "https://doi.org/10.1182/blood-2008-09-178707"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19096009"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19096009"}]}, {"type": "r", "ref": 23, "children": [{"type": "t", "text": "Jean-Rémy Courbard, Frédéric Fiore, José Adélaïde, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Interaction between two ubiquitin-protein isopeptide ligases of different classes, CBLC and AIP4/ITCH."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M206460200"}], "href": "https://doi.org/10.1074/jbc.M206460200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12226085"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12226085"}]}, {"type": "r", "ref": 24, "children": [{"type": "t", "text": "Tomasz Wegierski, Kerstin Hill, Michael Schaefer, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The HECT ubiquitin ligase AIP4 regulates the cell surface expression of select TRP channels."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO J (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.emboj.7601429"}], "href": "https://doi.org/10.1038/sj.emboj.7601429"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17110928"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17110928"}]}, {"type": "r", "ref": 25, "children": [{"type": "t", "text": "Naomi J Lohr, Jean P Molleston, Kevin A Strauss, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Human ITCH E3 ubiquitin ligase deficiency causes syndromic multisystem autoimmune disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Hum Genet (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ajhg.2010.01.028"}], "href": "https://doi.org/10.1016/j.ajhg.2010.01.028"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20170897"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20170897"}]}, {"type": "r", "ref": 26, "children": [{"type": "t", "text": "Dong Han, Yongjun Wang, Yabin Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The Tumor-Suppressive Human Circular RNA CircITCH Sponges miR-330-5p to Ameliorate Doxorubicin-Induced Cardiotoxicity Through Upregulating SIRT6, Survivin, and SERCA2a."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Circ Res (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1161/CIRCRESAHA.119.316061"}], "href": "https://doi.org/10.1161/CIRCRESAHA.119.316061"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32392088"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32392088"}]}, {"type": "r", "ref": 27, "children": [{"type": "t", "text": "Mingfang Tao, Peter C Scacheri, Jill M Marinis, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ITCH K63-ubiquitinates the NOD2 binding protein, RIP2, to influence inflammatory signaling pathways."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Curr Biol (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cub.2009.06.038"}], "href": "https://doi.org/10.1016/j.cub.2009.06.038"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19592251"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19592251"}]}, {"type": "r", "ref": 28, "children": [{"type": "t", "text": "Thomas Mund, Hugh R B Pelham "}, {"type": "b", "children": [{"type": "t", "text": "Control of the activity of WW-HECT domain E3 ubiquitin ligases by NDFIP proteins."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO Rep (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/embor.2009.30"}], "href": "https://doi.org/10.1038/embor.2009.30"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19343052"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19343052"}]}, {"type": "r", "ref": 29, "children": [{"type": "t", "text": "Thomas L Edwards, Virginia E Clowes, Hilda T H Tsang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Endogenous spartin (SPG20) is recruited to endosomes and lipid droplets and interacts with the ubiquitin E3 ligases AIP4 and AIP5."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem J (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1042/BJ20082398"}], "href": "https://doi.org/10.1042/BJ20082398"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19580544"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19580544"}]}, {"type": "r", "ref": 30, "children": [{"type": "t", "text": "Thomas Slagsvold, Adriano Marchese, Andreas Brech, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CISK attenuates degradation of the chemokine receptor CXCR4 via the ubiquitin ligase AIP4."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO J (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.emboj.7601267"}], "href": "https://doi.org/10.1038/sj.emboj.7601267"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16888620"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16888620"}]}, {"type": "r", "ref": 31, "children": [{"type": "t", "text": "Ziying Han, Cari A Sagum, Mark T Bedford, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ITCH E3 Ubiquitin Ligase Interacts with Ebola Virus VP40 To Regulate Budding."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Virol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/JVI.01078-16"}], "href": "https://doi.org/10.1128/JVI.01078-16"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27489272"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27489272"}]}, {"type": "r", "ref": 32, "children": [{"type": "t", "text": "Jacob J Adler, Brigitte L Heller, Lauren R Bringman, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Amot130 adapts atrophin-1 interacting protein 4 to inhibit yes-associated protein signaling and cell growth."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M112.446534"}], "href": "https://doi.org/10.1074/jbc.M112.446534"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23564455"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23564455"}]}, {"type": "r", "ref": 33, "children": [{"type": "t", "text": "Youngeun Kim, Wantae Kim, Yonghee Song, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Deubiquitinase YOD1 potentiates YAP/TAZ activities through enhancing ITCH stability."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1620306114"}], "href": "https://doi.org/10.1073/pnas.1620306114"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28416659"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28416659"}]}, {"type": "r", "ref": 34, "children": [{"type": "t", "text": "Richard Galinier, Evelyne Gout, Hugues Lortat-Jacob, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Adenovirus protein involved in virus internalization recruits ubiquitin-protein ligases."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochemistry (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1021/bi020125b"}], "href": "https://doi.org/10.1021/bi020125b"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12450395"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12450395"}]}, {"type": "r", "ref": 35, "children": [{"type": "t", "text": "François Lallemand, Su Ryeon Seo, Nathalie Ferrand, et al. "}, {"type": "b", "children": [{"type": "t", "text": "AIP4 restricts transforming growth factor-beta signaling through a ubiquitination-independent mechanism."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M500188200"}], "href": "https://doi.org/10.1074/jbc.M500188200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15946939"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15946939"}]}, {"type": "r", "ref": 36, "children": [{"type": "t", "text": "Frédéric Lévy, Katja Muehlethaler, Suzanne Salvi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ubiquitylation of a melanosomal protein by HECT-E3 ligases serves as sorting signal for lysosomal degradation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Cell (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1091/mbc.e04-09-0803"}], "href": "https://doi.org/10.1091/mbc.e04-09-0803"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15703212"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15703212"}]}, {"type": "r", "ref": 37, "children": [{"type": "t", "text": "Paola Infante, Roberta Faedda, Flavia Bernardi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Itch/β-arrestin2-dependent non-proteolytic ubiquitylation of SuFu controls Hedgehog signalling and medulloblastoma tumorigenesis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41467-018-03339-0"}], "href": "https://doi.org/10.1038/s41467-018-03339-0"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29515120"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29515120"}]}, {"type": "r", "ref": 38, "children": [{"type": "t", "text": "F Yang, K H Tay, L Dong, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Cystatin B inhibition of TRAIL-induced apoptosis is associated with the protection of FLIP(L) from degradation by the E3 ligase itch in human melanoma cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Death Differ (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/cdd.2010.29"}], "href": "https://doi.org/10.1038/cdd.2010.29"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20300110"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20300110"}]}, {"type": "r", "ref": 39, "children": [{"type": "t", "text": "Dan Levy, Nina Reuven, Yosef Shaul "}, {"type": "b", "children": [{"type": "t", "text": "A regulatory circuit controlling Itch-mediated p73 degradation by Runx."}]}, {"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.M803941200"}], "href": "https://doi.org/10.1074/jbc.M803941200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18701449"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18701449"}]}, {"type": "r", "ref": 40, "children": [{"type": "t", "text": "Flavia Scialpi, Martina Malatesta, Angelo Peschiaroli, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Itch self-polyubiquitylation occurs through lysine-63 linkages."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Pharmacol (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bcp.2008.07.028"}], "href": "https://doi.org/10.1016/j.bcp.2008.07.028"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18718449"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18718449"}]}, {"type": "r", "ref": 41, "children": [{"type": "t", "text": "Young Bong Choi, Noula Shembade, Kislay Parvatiyar, et al. "}, {"type": "b", "children": [{"type": "t", "text": "TAX1BP1 Restrains Virus-Induced Apoptosis by Facilitating Itch-Mediated Degradation of the Mitochondrial Adaptor MAVS."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.00422-16"}], "href": "https://doi.org/10.1128/MCB.00422-16"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27736772"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27736772"}]}, {"type": "r", "ref": 42, "children": [{"type": "t", "text": "Rohit Malik, Unice J K Soh, JoAnn Trejo, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Novel roles for the E3 ubiquitin ligase atrophin-interacting protein 4 and signal transduction adaptor molecule 1 in G protein-coupled receptor signaling."}]}, {"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.M111.336792"}], "href": "https://doi.org/10.1074/jbc.M111.336792"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22275353"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22275353"}]}, {"type": "r", "ref": 43, "children": [{"type": "t", "text": "Alessia Bellomaria, Gaetano Barbato, Gerry Melino, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Recognition mechanism of p63 by the E3 ligase Itch: novel strategy in the study and inhibition of this interaction."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Cycle (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.4161/cc.21918"}], "href": "https://doi.org/10.4161/cc.21918"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22935697"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22935697"}]}, {"type": "r", "ref": 44, "children": [{"type": "t", "text": "Chung-Pei Lee, Guan-Ting Liu, Hsiu-Ni Kung, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The Ubiquitin Ligase Itch and Ubiquitination Regulate BFRF1-Mediated Nuclear Envelope Modification for Epstein-Barr Virus Maturation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Virol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/JVI.01235-16"}], "href": "https://doi.org/10.1128/JVI.01235-16"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27466427"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27466427"}]}]}]}
Synonyms AIF4, ADMFD, DJ468O1.1, AIP4, NAPP1
Proteins ITCH_HUMAN
NCBI Gene ID 83737
API
Download Associations
Predicted Functions View ITCH's ARCHS4 Predicted Functions.
Co-expressed Genes View ITCH's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View ITCH's ARCHS4 Predicted Functions.

Functional Associations

ITCH has 9,185 functional associations with biological entities spanning 9 categories (molecular profile, organism, disease, phenotype or trait, chemical, functional term, phrase or reference, structural feature, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 130 datasets.

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

If available, associations are ranked by standardized value

Dataset Summary
Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles tissues with high or low expression of ITCH gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles tissues with high or low expression of ITCH gene relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray tissue samples with high or low expression of ITCH 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 ITCH 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 ITCH 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 ITCH 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 ITCH 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 ITCH gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
CCLE Cell Line Gene CNV Profiles cell lines with high or low copy number of ITCH 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 ITCH gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
CCLE Cell Line Proteomics Cell lines associated with ITCH protein from the CCLE Cell Line Proteomics dataset.
CellMarker Gene-Cell Type Associations cell types associated with ITCH 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 ITCH gene from the CHEA Transcription Factor Binding Site Profiles dataset.
ChEA Transcription Factor Targets transcription factors binding the promoter of ITCH 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 ITCH gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
ClinVar Gene-Phenotype Associations phenotypes associated with ITCH gene from the curated ClinVar Gene-Phenotype Associations dataset.
CMAP Signatures of Differentially Expressed Genes for Small Molecules small molecule perturbations changing expression of ITCH gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
COMPARTMENTS Curated Protein Localization Evidence Scores cellular components containing ITCH protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
COMPARTMENTS Curated Protein Localization Evidence Scores 2025 cellular components containing ITCH protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
COMPARTMENTS Experimental Protein Localization Evidence Scores cellular components containing ITCH protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
COMPARTMENTS Text-mining Protein Localization Evidence Scores cellular components co-occuring with ITCH 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 ITCH protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
CORUM Protein Complexes protein complexs containing ITCH protein from the CORUM Protein Complexes dataset.
COSMIC Cell Line Gene CNV Profiles cell lines with high or low copy number of ITCH gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
COSMIC Cell Line Gene Mutation Profiles cell lines with ITCH gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
CTD Gene-Disease Associations diseases associated with ITCH gene/protein from the curated CTD Gene-Disease Associations dataset.
dbGAP Gene-Trait Associations traits associated with ITCH gene in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
DepMap CRISPR Gene Dependency cell lines with fitness changed by ITCH gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
DISEASES Experimental Gene-Disease Association Evidence Scores 2025 diseases associated with ITCH gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
DISEASES Text-mining Gene-Disease Association Evidence Scores diseases co-occuring with ITCH 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 ITCH 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 ITCH gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
DisGeNET Gene-Phenotype Associations phenotypes associated with ITCH 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 ITCH 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 ITCH gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of ITCH 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 ITCH from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.
GAD Gene-Disease Associations diseases associated with ITCH gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
GAD High Level Gene-Disease Associations diseases associated with ITCH 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 ITCH gene relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.
GeneRIF Biological Term Annotations biological terms co-occuring with ITCH 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 ITCH from the GeneSigDB Published Gene Signatures dataset.
GEO Signatures of Differentially Expressed Genes for Diseases disease perturbations changing expression of ITCH 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 ITCH 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 ITCH 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 ITCH 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 ITCH 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 ITCH gene from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.
GO Biological Process Annotations 2015 biological processes involving ITCH gene from the curated GO Biological Process Annotations 2015 dataset.
GO Biological Process Annotations 2023 biological processes involving ITCH gene from the curated GO Biological Process Annotations 2023 dataset.
GO Biological Process Annotations 2025 biological processes involving ITCH gene from the curated GO Biological Process Annotations2025 dataset.
GO Cellular Component Annotations 2015 cellular components containing ITCH protein from the curated GO Cellular Component Annotations 2015 dataset.
GO Cellular Component Annotations 2023 cellular components containing ITCH protein from the curated GO Cellular Component Annotations 2023 dataset.
GO Cellular Component Annotations 2025 cellular components containing ITCH protein from the curated GO Cellular Component Annotations 2025 dataset.
GO Molecular Function Annotations 2015 molecular functions performed by ITCH gene from the curated GO Molecular Function Annotations 2015 dataset.
GO Molecular Function Annotations 2023 molecular functions performed by ITCH gene from the curated GO Molecular Function Annotations 2023 dataset.
GO Molecular Function Annotations 2025 molecular functions performed by ITCH gene from the curated GO Molecular Function Annotations 2025 dataset.
GTEx eQTL 2025 SNPs regulating expression of ITCH gene from the GTEx eQTL 2025 dataset.
GTEx Tissue Gene Expression Profiles tissues with high or low expression of ITCH 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 ITCH 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 ITCH gene relative to other tissue samples from the GTEx Tissue Sample Gene Expression Profiles dataset.
GWASdb SNP-Disease Associations diseases associated with ITCH gene in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
GWASdb SNP-Phenotype Associations phenotypes associated with ITCH 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 ITCH gene relative to other cell lines from the Heiser et al., PNAS, 2011 Cell Line Gene Expression Profiles dataset.
HPA Cell Line Gene Expression Profiles cell lines with high or low expression of ITCH 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 ITCH 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 ITCH 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 ITCH gene relative to other tissue samples from the HPA Tissue Sample Gene Expression Profiles dataset.
HPM Cell Type and Tissue Protein Expression Profiles cell types and tissues with high or low expression of ITCH protein relative to other cell types and tissues from the HPM Cell Type and Tissue Protein Expression Profiles dataset.
HPO Gene-Disease Associations phenotypes associated with ITCH gene by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hub Proteins Protein-Protein Interactions interacting hub proteins for ITCH from the curated Hub Proteins Protein-Protein Interactions dataset.
HuGE Navigator Gene-Phenotype Associations phenotypes associated with ITCH gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
IMPC Knockout Mouse Phenotypes phenotypes of mice caused by ITCH gene knockout from the IMPC Knockout Mouse Phenotypes dataset.
InterPro Predicted Protein Domain Annotations protein domains predicted for ITCH protein from the InterPro Predicted Protein Domain Annotations dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of ITCH gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset.
KEA Substrates of Kinases kinases that phosphorylate ITCH protein from the curated KEA Substrates of Kinases dataset.
KEGG Pathways pathways involving ITCH protein from the KEGG Pathways dataset.
Kinase Library Serine Threonine Kinome Atlas kinases that phosphorylate ITCH protein from the Kinase Library Serine Threonine Atlas dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of ITCH 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 ITCH 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 ITCH 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 ITCH 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 ITCH gene from the LINCS L1000 CMAP Chemical Perturbations Consensus Signatures dataset.
LINCS L1000 CMAP CRISPR Knockout Consensus Signatures gene perturbations changing expression of ITCH 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 ITCH gene from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
LOCATE Curated Protein Localization Annotations cellular components containing ITCH 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 ITCH protein from the LOCATE Predicted Protein Localization Annotations dataset.
MGI Mouse Phenotype Associations 2023 phenotypes of transgenic mice caused by ITCH gene mutations from the MGI Mouse Phenotype Associations 2023 dataset.
MiRTarBase microRNA Targets microRNAs targeting ITCH 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 ITCH 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 ITCH gene relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
MSigDB Signatures of Differentially Expressed Genes for Cancer Gene Perturbations gene perturbations changing expression of ITCH gene from the MSigDB Signatures of Differentially Expressed Genes for Cancer Gene Perturbations dataset.
NIBR DRUG-seq U2OS MoA Box Gene Expression Profiles drug perturbations changing expression of ITCH gene from the NIBR DRUG-seq U2OS MoA Box dataset.
NURSA Protein Complexes protein complexs containing ITCH protein recovered by IP-MS from the NURSA Protein Complexes dataset.
NURSA Protein-Protein Interactions interacting proteins for ITCH from the NURSA Protein-Protein Interactions dataset.
OMIM Gene-Disease Associations phenotypes associated with ITCH gene from the curated OMIM Gene-Disease Associations dataset.
PANTHER Pathways pathways involving ITCH protein from the PANTHER Pathways dataset.
Pathway Commons Protein-Protein Interactions interacting proteins for ITCH from the Pathway Commons Protein-Protein Interactions dataset.
PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations gene perturbations changing expression of ITCH 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 ITCH gene from the PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
PFOCR Pathway Figure Associations 2023 pathways involving ITCH protein from the PFOCR Pathway Figure Associations 2023 dataset.
PFOCR Pathway Figure Associations 2024 pathways involving ITCH protein from the Wikipathways PFOCR 2024 dataset.
Phosphosite Textmining Biological Term Annotations biological terms co-occuring with ITCH protein in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
PhosphoSitePlus Substrates of Kinases kinases that phosphorylate ITCH protein from the curated PhosphoSitePlus Substrates of Kinases dataset.
PID Pathways pathways involving ITCH protein from the PID Pathways dataset.
Reactome Pathways 2014 pathways involving ITCH protein from the Reactome Pathways dataset.
Reactome Pathways 2024 pathways involving ITCH protein from the Reactome Pathways 2024 dataset.
Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures gene perturbations changing expression of ITCH 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 ITCH 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 ITCH 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 ITCH 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 ITCH 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 ITCH gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
RummaGEO Drug Perturbation Signatures drug perturbations changing expression of ITCH gene from the RummaGEO Drug Perturbation Signatures dataset.
RummaGEO Gene Perturbation Signatures gene perturbations changing expression of ITCH gene from the RummaGEO Gene Perturbation Signatures dataset.
Sanger Dependency Map Cancer Cell Line Proteomics cell lines associated with ITCH protein from the Sanger Dependency Map Cancer Cell Line Proteomics dataset.
Tahoe Therapeutics Tahoe 100M Perturbation Atlas drug perturbations changing expression of ITCH gene from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
TargetScan Predicted Conserved microRNA Targets microRNAs regulating expression of ITCH gene predicted using conserved miRNA seed sequences from the TargetScan Predicted Conserved microRNA Targets dataset.
TargetScan Predicted Nonconserved microRNA Targets microRNAs regulating expression of ITCH 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 ITCH 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 ITCH protein from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
TISSUES Curated Tissue Protein Expression Evidence Scores 2025 tissues with high expression of ITCH protein from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
TISSUES Experimental Tissue Protein Expression Evidence Scores tissues with high expression of ITCH 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 ITCH 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 ITCH 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 ITCH protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Virus MINT Protein-Viral Protein Interactions interacting viral proteins for ITCH from the Virus MINT Protein-Viral Protein Interactions dataset.
Virus MINT Protein-Virus Interactions viruses interacting with ITCH from the Virus MINT Protein-Virus Interactions dataset.
WikiPathways Pathways 2014 pathways involving ITCH protein from the Wikipathways Pathways 2014 dataset.
WikiPathways Pathways 2024 pathways involving ITCH protein from the WikiPathways Pathways 2024 dataset.