| Name | TP53 target 3D |
| Description | Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nA wide array of recent studies (e.g."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "10"}]}, {"type": "t", "text": "has provided deep insights into diverse cellular processes. These investigations have defined the roles of key transcription factors—such as members of the LIM homeobox family (Lhx6, Lhx8, and Lhx7)—in the specification, differentiation, migration, and maturation of various neuronal subtypes (see also."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "11", "end_ref": "15"}]}, {"type": "t", "text": " Equally, other studies have illuminated the functions of accessory subunits of voltage‐gated calcium channels (including CACNA2D2 and related proteins) as well as mitochondrial ATP‐binding cassette transporters (such as ABCB6) in controlling calcium currents, synaptic organization, and intracellular porphyrin trafficking."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "16", "end_ref": "20"}]}, {"type": "t", "text": " Additional studies have focused on regulators of genomic stability and tumorigenesis (for example, BCCIP), highlighting that only transient loss of function in essential caretaker genes may initiate transformation while their complete loss remains incompatible with viability."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "21", "end_ref": "23"}]}, {"type": "t", "text": " Other works extend these findings to specialized contexts such as sleep regulation, craniofacial and tooth development, and responses to environmental toxicants"}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "24", "end_ref": "36"}]}, {"type": "t", "text": "that broaden our knowledge of developmental regulation and disease mechanisms.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nNotably, despite the breadth of these investigations spanning neurodevelopment, synaptic organization, ion channel regulation, mitochondrial function, and genomic integrity, none of the provided abstracts specifically mention or analyze TP53TG3D. Consequently, while the research collectively enriches our understanding of cell fate determination, calcium‐dependent signaling, and tumor suppressor pathways, there is no evidence from these studies to assign a functional role to TP53TG3D. In this context, any summary of TP53TG3D function would be speculative because the conserved themes—spanning p53-related networks and cellular stress responses—are not directly discussed with regard to TP53TG3D in the available literature."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "37"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Jens Brodbeck, Anthony Davies, Jo-Maree Courtney, et al. 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| Synonyms | TP53TG3B |
| NCBI Gene ID | 729264 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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TP53TG3D has 810 functional associations with biological entities spanning 3 categories (disease, phenotype or trait, cell line, cell type or tissue, gene, protein or microRNA) extracted from 11 datasets.
Click the + buttons to view associations for TP53TG3D from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of TP53TG3D gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| CellMarker Gene-Cell Type Associations | cell types associated with TP53TG3D gene from the CellMarker Gene-Cell Type Associations dataset. | |
| ChEA Transcription Factor Targets 2022 | transcription factors binding the promoter of TP53TG3D gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of TP53TG3D gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 | diseases co-occuring with TP53TG3D gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of TP53TG3D gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| GTEx Tissue Sample Gene Expression Profiles | tissue samples with high or low expression of TP53TG3D gene relative to other tissue samples from the GTEx Tissue Sample Gene Expression Profiles dataset. | |
| HPA Tissue Gene Expression Profiles | tissues with high or low expression of TP53TG3D gene relative to other tissues from the HPA Tissue Gene Expression Profiles dataset. | |
| HPA Tissue Sample Gene Expression Profiles | tissue samples with high or low expression of TP53TG3D gene relative to other tissue samples from the HPA Tissue Sample Gene Expression Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of TP53TG3D gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| Rummagene Transcription Factor Associations 2026 | transcription factors regulating expression of TP53TG3D gene from the Rummagene Transcription Factor Associations 2026 dataset. | |