GSTT4 Gene

Name glutathione S-transferase theta 4
Description Predicted to enable glutathione transferase activity. Predicted to be involved in glutathione metabolic process. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe set of provided abstracts addresses diverse mechanisms underlying cell–cell junction formation, inflammation‐related signaling pathways, and transcriptional regulation in a number of physiological and pathological contexts, including renal magnesium and calcium transport, oncogenic proliferation, and fibrogenesis. For example, several studies detail how claudin‐16 and claudin‐19 interact to assemble tight junction structures that govern cation-selective paracellular transport in the kidney."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nOther contributions focus on the activation of oncogenic and inflammatory signaling pathways—illustrated by the constitutive signaling of the viral receptor US28 that triggers the IL-6–JAK1–STAT3 cascade"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "—and on the regulatory actions of transcription factor complexes such as STRA13 and the Elongator complex subunit ELP2 (also known as STAT3-interacting protein 1). These proteins are implicated in processes ranging from apoptosis, osteoblast differentiation, and even neurodevelopment."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "6", "end_ref": "10"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nA further study highlights novel roles for a circular RNA derived from ELP2 (circELP2) in promoting pulmonary fibrogenesis via microRNA sponging and downstream regulation of mitochondrial quality control."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "11"}]}, {"type": "t", "text": " It is important to note, however, that none of these abstracts provide any information regarding GSTT4. Despite the rich discussion of proteins governing tight junction integrity, inflammatory cascades, and transcriptional modulation, the function of GSTT4 is not addressed in this collection of studies.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "A V Ivanova, S V Ivanov, X Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "STRA13 interacts with STAT3 and modulates transcription of STAT3-dependent targets."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Mol Biol (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jmb.2004.05.025"}], "href": "https://doi.org/10.1016/j.jmb.2004.05.025"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15223310"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15223310"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Jianghui Hou, Aparna Renigunta, Antonio S Gomes, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Claudin-16 and claudin-19 interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.0907724106"}], "href": "https://doi.org/10.1073/pnas.0907724106"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19706394"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19706394"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Henrik Dimke, Camille Griveau, Wung-Man Evelyne Ling, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Claudin-19 localizes to the thick ascending limb where its expression is required for junctional claudin-16 localization."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Ann N Y Acad Sci (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/nyas.15014"}], "href": "https://doi.org/10.1111/nyas.15014"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37344378"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37344378"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Hiroaki Okuda, Takayuki Manabe, Takeshi Yanagita, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Novel interaction between HMGA1a and StIP1 in murine terminally differentiated retina."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Neurosci (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.mcn.2006.06.009"}], "href": "https://doi.org/10.1016/j.mcn.2006.06.009"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16870469"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16870469"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Erik Slinger, David Maussang, Andreas Schreiber, et al. "}, {"type": "b", "children": [{"type": "t", "text": "HCMV-encoded chemokine receptor US28 mediates proliferative signaling through the IL-6-STAT3 axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Signal (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1126/scisignal.2001180"}], "href": "https://doi.org/10.1126/scisignal.2001180"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20682912"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20682912"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "John M Luk, Man-Kit Tong, Bobo W Mok, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Sp1 site is crucial for the mouse claudin-19 gene expression in the kidney cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS Lett (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.febslet.2004.11.010"}], "href": "https://doi.org/10.1016/j.febslet.2004.11.010"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15589828"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15589828"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Chang-Peng Xu, Xue Li, Yan-Jun Hu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Quantitative proteomics reveals ELP2 as a regulator to the inhibitory effect of TNF-α on osteoblast differentiation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Proteomics (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jprot.2014.11.002"}], "href": "https://doi.org/10.1016/j.jprot.2014.11.002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25486498"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25486498"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Yasunori Saitoh, Hiroshi Suzuki, Kazutoshi Tani, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Tight junctions. Structural insight into tight junction disassembly by Clostridium perfringens enterotoxin."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Science (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1126/science.1261833"}], "href": "https://doi.org/10.1126/science.1261833"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25678664"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25678664"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Shan Lu, Hong-Wu Fan, Kai Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Suppression of Elp2 prevents renal fibrosis and inflammation induced by unilateral ureter obstruction (UUO) via inactivating Stat3-regulated TGF-β1 and NF-κB pathways."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2018.04.227"}], "href": "https://doi.org/10.1016/j.bbrc.2018.04.227"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29723529"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29723529"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Marija Kojic, Tomasz Gawda, Monika Gaik, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotype."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41467-021-22888-5"}], "href": "https://doi.org/10.1038/s41467-021-22888-5"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33976153"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33976153"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Songzi Zhang, Diwei Tu, Weili Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "circELP2 reverse-splicing biogenesis and function as a pro-fibrogenic factor by targeting mitochondrial quality control pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Mol Med (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/jcmm.18098"}], "href": "https://doi.org/10.1111/jcmm.18098"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38159063"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38159063"}]}]}]}
NCBI Gene ID 25774
API
Download Associations
Predicted Functions View GSTT4's ARCHS4 Predicted Functions.
Co-expressed Genes View GSTT4's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View GSTT4's ARCHS4 Predicted Functions.

Functional Associations

GSTT4 has 958 functional associations with biological entities spanning 6 categories (chemical, functional term, phrase or reference, disease, phenotype or trait, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 17 datasets.

Click the + buttons to view associations for GSTT4 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles tissue samples with high or low expression of GSTT4 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
Carcinogenome Chemical Perturbation Carcinogenicity Signatures small molecule perturbations changing expression of GSTT4 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
CM4AI KOLF21J CRISPRi Gene Perturbation Atlas gene perturbations changing expression of GSTT4 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset.
COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 cellular components co-occuring with GSTT4 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 diseases co-occuring with GSTT4 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
GO Biological Process Annotations 2025 biological processes involving GSTT4 gene from the curated GO Biological Process Annotations2025 dataset.
GO Molecular Function Annotations 2025 molecular functions performed by GSTT4 gene from the curated GO Molecular Function Annotations 2025 dataset.
GTEx eQTL 2025 SNPs regulating expression of GSTT4 gene from the GTEx eQTL 2025 dataset.
GTEx Tissue Gene Expression Profiles 2023 tissues with high or low expression of GSTT4 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.
GWAS Catalog SNP-Phenotype Associations 2025 phenotypes associated with GSTT4 gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
JASPAR Predicted Human Transcription Factor Targets 2025 transcription factors regulating expression of GSTT4 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 GSTT4 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset.
KEGG Pathways 2026 pathways involving GSTT4 protein from the KEGG Pathways 2026 dataset.
Rummagene Transcription Factor Associations 2026 transcription factors regulating expression of GSTT4 gene from the Rummagene Transcription Factor Associations 2026 dataset.
RummaGEO Drug Perturbation Signatures drug perturbations changing expression of GSTT4 gene from the RummaGEO Drug Perturbation Signatures dataset.
RummaGEO Gene Perturbation Signatures gene perturbations changing expression of GSTT4 gene from the RummaGEO Gene Perturbation Signatures dataset.
TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 tissues co-occuring with GSTT4 protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.